View
1
Download
0
Category
Preview:
Citation preview
Page 1 of 49
AMENDMENT TO PREBID MEETING HELD ON DT. 16.03.2019 OF THE TENDER FOR SUPPLY & INSTALLATION OF CARDIOLOGY, RADIOLOGY & ANESTHESIA EQUIPMENT’S AT CARDIAC CARE HOSPITAL, JHARSUGUDA AND AT SCBMCH-CUTTACK Bid Ref. No.: OSMCL/2018-19/CARDIAC CARE/31
• Total No. of prospective bidders/ representatives present in the pre-bid meeting are Twenty Five (25).
• The amendment to technical specification of the tender items and techno-commercial points is attached at
Annexure-A and Annexure-B.
Annexure-A
AMENDMENT TO TECHNICAL SPECIFICATION
Queries raised and received from
the prospective bidders
Original Technical
Specification
Clarifications/
Amendments in response
to the queries.
ITEM NO.1 (CATH LAB) AND ITEM NO.2 (CATH LAB (for SCB))
Under Operational Requirement,
The requirement of 3D Rotational
Angiography and area of application
may be specified.
Or
Requested to delete this point.
Under Operational Requirement,
3D Rotational Angiography should
be available.
Amended
The requirement of “3D
Rotational Angiography” is
deleted from the
specification.
Pg.58 &63 1. Gantry (Pt.no.1):
Celling/ floor mounted gantry providing
full body coverage without repositioning
of patient. Gantry must have 3 working
position for easy operation
Celling /Floor mounted gantry
providing full body coverage
without repositioning of patient.
Gantry must have 0, 90, -90deg
working position for easy
operation from 3 sides of the
patient
Amended
Celling/ floor mounted gantry
providing full body coverage
without repositioning of
patient. Gantry must have 3
working position for easy
operation.
Pg.58&63 1. Gantry (Pt.no.2):
Facility for motorized positioning/
rotation of stand may be either from
the ceiling or from floor pivot.
Or
The point may be deleted.
Or
Generalize as movement should be
manual with electromagnetic locking
mechanism.
Facility for motorized
positioning/rotation of stand from
the ceiling pivot by +/-90 degrees
for improved workflow
Amended
Facility for motorized
positioning/rotation of stand
from the ceiling or floor pivot
by +/-90 degrees for
improved workflow.
Pg.58&63 1. Gantry (Pt.no.2):
Patient access must be possible from
either left or right side. 15 deg. /sec or
higher rotation speed with non-contact
sensing mechanism.
Or
Patient access must be possible from
either left or right side. 25 deg. /sec or
Patient access must be possible
from either left or right side. 25
deg. /sec or higher rotation speed
with non-contact sensing
mechanism.
Amended
Patient access must be
possible from either left or
right side. 25 deg. /sec or
higher rotation speed with
non-contact sensing
mechanism or collision
protection switches.
Page 2 of 49
higher rotation speed with non-contact
sensing mechanism or collision
protection switches.
Pg.59&63 1.Gantry (Pt.no.2):
Gantry rotation (Cranial-to-caudal)
angulation cannot be +/- 120 deg. and
+/- 90 deg. respectively.
Or
LAO/RAO +/-120 deg. and Cranial to
caudal+/- 45deg
Rotational angle +90 degree and -90
degree and orbital angle +45 degree
and -45 degree
Or
Rotational angle: RAO120 to LAO 120,
Sliding Angle: CRA 50 to CAU 90
Gantry rotation (Cranial-to-
caudal) angulation +/- 120 deg.
and +/- 90 deg. respectively.
Amended
Gantry rotation (Cranial-to-
caudal) angulation should be
+/- 45 deg. and LAO and
RAO should be +/- 120 deg.
and +/- 90deg. respectively.
Pg.59&63 1.Gantry (Pt.no.4):
The throat depth of the gantry should
be 90cm or more.
The throat depth of the gantry
must be 100cm or more for better
groin access.
Amended
The throat depth of the
gantry should be 90cm or
more.
Pg.59&64 2.Table (Pt.no.6):
Extendable arm rest both sides and
Elbow guard. Motorized up/down, free
floating 4way table top, least radiation
attenuation, at least 250 kg. instead of
200Kg. + at least 100kgs of additional
weight for resuscitation in the metal
free overhang area without having to
retract the table back on its base.
Extendable arm rest both sides
and Elbow guard. Motorized
up/down, free floating 4way table
top, least radiation attenuation, at
least 200 kg + at least 100kgs of
additional weight for resuscitation
in the metal free overhang area
without having to retract the
table back on its base.
No Change
Pg.59&64 2.Table (Pt.no.8):
Table tilting movement may be deleted.
At least +/- 15degree tilt must be
possible. No Change
Pg.59&64 2.Table (Pt.no.9):
Motorized longitudinal imaging
coverage should be 120cm or more
Motorized longitudinal travel
120cm or more.
No Change
Pg.59&64 2.Table (Pt.no.10):
Transverse Travel +/-14 cm or more
Manual transverse travel +/-
17.5cm or more.
Amended
Manual transverse travel +/-
14cm or more.
Pg.59&64 2.Table (Pt.no.10):
Accessories with table and
mattress:
Remove or make it optional
Accessories with table and
mattress:
Peripheral filter set
Amended
Peripheral filter set or any
equivalent technique for
same purpose should be
available.
Pg.59&64 3.Detector (Pt.no.1):
Detector size may be 30x30cm instead
of 30x40cm detector.
Or
A 30 x 40cm rectangular detector
that can be rotated by 90 degrees
for better flexibility and projection
angles depending upon area of
No change
Page 3 of 49
20 X 20 cm or more square digital flat
panel detector for all projections
depending on area of interest.
interest.
Pg.59&64 3.Detector (Pt.no.2):
The digital output of the flat detector
may be is 2k x 2k image matrix instead
of 2k x 2.5k at 16 bits instead of 14bit
depth.
14bit (Toshiba)
Or
Flat Detector of latest generation, the
digital output of the flat detector must
be is 1k x 1k image matrix at 14 bits
depth for the largest mode
Or
Flat Detector of latest generation, the
digital output of the flat detector must
be is 2k x 2.5k image matrix at 16 bits
depth for the largest mode.
Flat Detector of latest generation,
the digital output of the flat
detector must be is 2k x 2.5k
image matrix at 14 bits depth for
the largest mode.
Amended
Flat detector of latest
generation, the digital output
of the flat detector must be is
2k x 2k image matrix at 16
bits depth for the largest
mode.
Pg.59&64 3.Detector (Pt.no.3):
System must have at least 4 imaging
modes.
System must have at least six
imaging modes. No change
Pg.60&64 3.Detector (Pt.no.5):
Minimum pixel pitch may be of at least
194 x 194 microns or lower instead of
160 micron or lower.
Or
Pixel size should be 200 microns or less.
Or
Min. pixel pitch of at least 194
(microns) or lower for better resolution.
Min. pixel pitch of at least 160
(microns) or lower for better
resolution.
No change
Pg.60&64 4.Image Processing &
Storage (Pt.no.5):
System must have a fully digital 1K
image processing for improved detailed
visualization of small structures
Or
System must have a fully digital 1K
image processing for improved detailed
visualization of small structures. System
must have storage capability of at least
1,00,000 images at matrix size of 1024
x 1024.
System must have a fully digital
2K image processing for improved
detailed visualization of small
structures.
Amended
System must have a fully
digital 1K or 2K image
processing for improved
detailed visualization of small
structures.
Pg.60&65 5. X-ray Generator:
Pulsed X-ray for (subtracted) acquisition
up to 30 frames/sec. for vascular
applications.
Pulsed X-ray for (subtracted)
acquisition up to 6 frames/sec. for
vascular applications.
No Change
Page 4 of 49
Pg.60&65 6. Tube (Pt.no.1):
A noise-free, water/oil cooled, dual
focus rotating anode x-ray tube with
spiral groove bearing technology and
fluid lubricant/ closed loop water chiller
for faster cooling must be provided.
A noise-free, oil cooled, dual
focus rotating anode x-ray tube
with spiral groove bearing
technology and fluid lubricant for
faster cooling must be provided.
No Change
Pg.60&65 6. Tube
Tube power should be 80KW or more. Additional point for X-ray tube. No Change
Pg.60&65 6. Tube (Pt.no.2):
Minimum Anode Heat Capacity may be
3.5 MHU or more instead of 2.4 MHU or
more
Or
5MHU or more
Or 3MHU or more
Minimum Anode Heat Capacity:
2.4 MHU or more
Amended
Minimum Anode Heat
Capacity: 3 MHU or more
Pg.60&65 6. Tube (Pt.no.3):
Cooling rate or Anode Heat Dissipation
of x-ray tube should be 900 kHU/min or
more
Or
Cooling rate or Anode Heat Dissipation
of x-ray tube must be 460 kHU/min or
more.
Cooling rate or Anode Heat
Dissipation of x-ray tube must be
more 500 kHU.
Amended
Cooling rate or Anode heat
dissipation of x-ray tube must
be 500 kHU or more.
Pg.60&65 6. Tube (Pt.no.4):
X-ray tube may have primary or
secondary grid switching.
Or
X-ray tube must have secondary/ inbuilt
grid switching.
X-ray tube must have secondary
grid switching.
Amended
X-ray tube should have
primary or secondary grid
switching or inbuilt grid
switching.
Pg.60&65 6. Tube (Pt.no.5):
Deliverable power may be 3000W on
continuous fluoro power instead of
3200W.
Or
System must be capable of delivering
minimum 2200W continuous fluoro
power.
System must be capable of
delivering minimum 3200W
continuous fluoro power.
Amended
System should be capable of
delivering minimum 2200W
continuous fluoro power.
Pg.60&65 6. Tube (Pt.no.6):
Additional beam filtration of at least 1.0
mm Al/Cu equivalent.
Different filter sizes and types to be
freely selectable at the table side for
any patient weight for maximum
radiation safety to staff and patients.
Additional beam filtration of at
least 1.0 mm Cu equivalent.
Different filter sizes and types to
be freely selectable at the table
side for any patient weight for
maximum radiation safety to staff
and patients.
Amended
Additional beam filtration of
at least 1.0 mm Al/Cu
equivalent.
Different filter sizes and types
to be freely selectable at the
table side for any patient
weight for maximum
radiation safety to staff and
patients.
Page 5 of 49
Pg.60&65 6. Tube (Pt.no.10):
The point should be deleted.
Parallel display of live and
roadmap image for optimal guide-
wire navigation.
No Change
Pg.61&66 7. Image Display
Monitors (Pt.no.1):
Four/Six LCD/TFT flat 19 inch may be
supplied instead of Two monitors/
System should have 55inch or more
large monitor to display live image,
reference & hemodynamic
Or
Two backup monitors for live and
reference
Two LCD/TFT flat 19inch
Monochrome Monitors with wide -
viewing angle, high luminance,
high contrast, flicker free,
distortion-free: one for live image
& one for reference.
Amended
Four/Six LCD/TFT flat 19inch
monochrome monitors with
wide -viewing angle, high
luminance, high contrast,
flicker free, distortion-free:
one for live image & one for
reference.
Pg.62&67 Accessories (Pt.no.8):
The point “Radiation protection Visor
X4” may be clarified.
Radiation protection Visor X4
Amended
The point “Radiation
protection Visor X4” should
be understood as Lead
goggles for vision protection.
Pg.58&67 Operational
Requirement (Pt.no.17):
Lead-free aprons may be asked.
Lead aprons: 6nos. should be
supplied.
Amended
Lead-free aprons: 6nos.
should be supplied.
Pg. 61&66 Quantification Software
Suggestion to add: The system should
have stent Enhancement software with
fade and fade out and it should be
operated in the control room.
Additional specification to
Quantification Software
Amended
The system should have
stent enhancement software
with fade and fade out and it
should be operated in the
control room.
Pg. 61&66 Quantification Software
Suggestion to add: FFR License
Additional specification to
Quantification Software
Amended
The system should have FFR
license.
Pg. 61&66 Image Display Monitors
(Pt. no.4):
Monitors brightness should be at least
800 cd/m2 instead of 600 cd/m2.
Monitors brightness should be at
least 600 cd/m2
Amended
Monitors brightness should
be at least 600 cd/m2 or
more.
ITEM NO.3 (IABP- INTRA AORTIC BALLOON PUMP)
Pg.70 System Configuration
(Pt.no.4.3):
Intra Aortic Balloon Catheter for adults,
Size 34cc may be amended to
30cc/34cc- 4nos., Size: 40cc - Qty: 6
Nos. Reusable Invasive Blood pressure
transducer system with pressure flush
device system. Qty: 2 Nos.
Intra Aortic Balloon Catheter for
Adults, Size: 34cc - Qty: 4 Nos,
Size: 40cc - Qty: 6 Nos. Reusable
Invasive Blood pressure
transducer system with pressure
flush device system. Qty: 2 Nos.
Amended
Intra Aortic Balloon Catheter
for Adults, Size: 30cc/34cc -
Qty: 4 Nos, Size: 40cc - Qty:
6 Nos. Reusable Invasive
Blood pressure transducer
system with pressure flush
device system. Qty: 2 Nos.
ITEM NO.4 (3D ECHO MACHINE WITH TEE)
Pg.72 Technical Specification
(Point. No 6)
The clause should be removed as it will
System should be capable of
supporting LIVE 3D matrix
No Change
Page 6 of 49
restrict participation. transducer capable of supporting
up-to 2000 elements for
exceptional LIVE 3D image quality
on the matrix array transducer.
Pg.72 Technical Specification
(Point. No.9)
The clause should be removed as it is
vendor specific.
System should offer LIVE X –
Plane imaging with manipulation
of orthogonal plane-lateral,
elevation and rotation should be
possible. Elevation beam steering
should be possible so that ideal
en-face views for measurements
can be obtained without moving
the transducer.
No Change
Pg.72 Technical Specification
(Point. No.17)
The clause should be removed as it is
vendor specific.
Based strain like VVI, AFT and
TMQ should be offered. These
should be offered both OFF-LINE
as well as online.
No Change
Pg.72 Technical Specification
(Point. No 20)
Should have great ergonomic design
with dual touch control panel of
minimum size 10-11 inches, which is
comfortable and convenient to avoid
user muscle strain & stress injuries.
System should have a 21-inches high
resolution flat panel medical grade
display monitor with nearly infinite
position adjustment
Or
System should have a 22 -inch high
resolution flat panel medical grade
display monitor with nearly infinite
position adjustment.
Should have great ergonomic
design, with dual touch control
panel of minimum size-10-11
inches, which is comfortable and
convenient to avoid user muscle
strain & stress injuries. System
should have a 24-inch high
resolution flat panel medical
grade display monitor with nearly
infinite position adjustment
Amended
Should have great ergonomic
design, with dual touch
control panel of minimum
size 10 to 11 inches, which is
comfortable and convenient
to avoid user muscle strain &
stress injuries.
System should have atleast
21inch or more high-
resolution flat panel medical
grade display monitor with
nearly infinite position
adjustment.
Pg.72 Technical Specification
(Pt.no.26):
Hard disk capacity of 5TB may not be
available.
System should have storage
facility of images, loops in the
hard disk drive of 5 TB or more.
System should be able to transfer
Images & clips to CD& DVD
media.
Amended
System should have storage
facility of images, loops in the
hard disk drive of 1 TB or
more System should be able
to transfer Images & clips to
CD & DVD media.
Pg.72 Technical Specification
(Pt.no.26.e):
Should have 2D Convex Probe
Convex Array Matrix Transducer
for adult LIVE 3D with frequency
ranging from 1-5 MHz.
No Change
Page 7 of 49
ITEM NO.5 (ULTRASOUND MACHINE WITH COLOR DOPPLER)
Pg.74 Product Quality Standard:
Both the machine and the real time
shear wave electrography should be
USA FDA certified.
Should be USFDA and European
CE approved product.
Amended
The whole system along with
probes should be USFDA and
European CE approved.
Pg.74 Technical Specification (Pt.
no.3):
Digital processing channels should be
more than 4,00,000
The system should have 60,000
or more digital processing
channels.
No Change
Pg.74 Technical Specification (Pt.
no.7):
The system should have a frame rate
on receive of over 2500 frames per
second or more
The system should have a frame
rate on receive of over 5000
frames per second or more.
No Change
System should have fusion and
navigation software as a standard part
of configuration or upgradation should
be available.
Additional point to specification No Change
Pg.75 Technical Specification (Pt.
no. 19, bullet pt.1):
Should have real time shear wave
elastography mode capable of
performing Real time Shear Wave tissue
elastography imaging with convex and
linear probe.
The real time shear wave
elastography mode should be
capable of performing;
Real time Shear Wave tissue
elastography imaging with
convex, linear, 3D, micro convex
and endocavity transducers.
Amended
Should have shear wave
elastography mode capable
of performing Real time
Shear Wave tissue
elastography imaging on
convex and linear probe.
Pg.75 Technical Specification (Pt.
no. 19, bullet pt.5):
User adjustable elasticity-box size with
a Display Depth should be 0 to 8cm or
more instead of 0 - 12cm.
Should be User adjustable
elasticity-box size with a Display
Depth: 0 - 12cm
Amended
Should be user adjustable
elasticity-box size with a
display depth: 0 to 8cm or
more.
Pg.75 Technical Specification (Pt.
no. 19, bullet pt.6):
Point need to be deleted
Elastography Quantification
should be available with pixel
accurate absolute or discreet
Elasticity values on all
transducers.
Amended
The feature of elastography
quantification should be
available with pixel accurate
absolute or discrete elasticity
values.
Pg.75 Technical Specification (Pt.
no. 27, bullet pt.6):
Convex transducer should be single
crystal type.
All the transducers are of single
crystal type.
No Change
Convex and linear transducer
should be single crystal type.
Following features should be
added
• Elastography on Convex Probe &
Linear Probe
• System should have 4 active probe
ports
Additional point to specification
Amended
System should have atleast 4
active ports.
Page 8 of 49
ITEM NO.6 (PORTABLE ECHO)
Pg.77 Technical Specification (Pt.
no. 3):
System weight should be maximum
7.5kg. or less with the internal battery.
The system should be very light
with maximum of 6.5 kgs.
Amended
The system should be very
light with maximum of 7.5
kg. or less with internal
battery but without the probe
attached.
Pg.77 Technical Specification (Pt.
no. 5):
Display size may be 15inch or more
instead of 17inch.
System must have minimum 17
inch high resolution integrated
flat panel display monitor with
minimum monitor resolution of
1050 x 1040.
Amended
System must have minimum
15 inch or more high
resolution integrated flat
panel display monitor with
minimum monitor resolution
of 1050 x 1040.
Display size may be 14inch or more
instead of 17inch.
Pg.77 Technical Specification (Pt.
no. 5):
System must be offered with 2D M-
mode, color M-mode, anatomical M-
mode, color flow, pulse wave doppler,
continuous wave Doppler and
directional color power Doppler
System Must be offered with 3D
M-mode, color M-mode,
anatomical M-mode, color flow,
pulse wave Doppler, continuous
wave Doppler and directional
color power Doppler
Amended
System must be offered with
2D M-mode, color M-mode,
anatomical M-mode, color
flow, pulse wave Doppler,
continuous wave Doppler and
directional color power
doppler and tissue doppler
imaging.
Pg.77 Technical Specification (Pt.
no. 14):
3D frame is not applicable for such
system.
System must be offered with 3D
frame rate of at least 750
frames/second. Acquisition frame
rate should be clearly mentioned
in the technical quote.
Amended
System must be offered with
2D frame rate of at least 750
frames/second. Acquisition
frame rate should be clearly
mentioned in the technical
quote.
Pg.78 Technical Specification (last
point)
Requirement of TEE probes may be
clearly specified.
Should be compatible with TEE
probes supplied with the main
machine
Amended
Should be compatible with
TEE probes supplied with the
main machine and separate
TEE probe should also be
quoted and supplied. The
cost of the TEE probe shall
have to be quoted in
separate price bid format in
pdf file (Format-B) as unit
price breakup quoted in the
excel BoQ file.
ITEM NO.7 (PORTABLE COLOR DOPPLER ULTRASOUND MACHINE)
Pg.78 Technical Specification (Pt.
no. 11)
Flat LCD/TFT monitor of at least 14” or
more with flicker free image
Flat LCD/TFT monitor of at least
17inch with flicker free image. No Change
Page 9 of 49
Pg.79 Technical Specification (Pt.
no. 11)
Battery capacity may be at least 30
minutes or more instead of 2hours.
On-board storage of at least
10,000 images, USB port for
connectivity to computer. Should
be able to operate both on AC
and battery. Battery pack should
be self-recharging and should last
at least for 2 hours when fully
charged.
Amended
On-board storage of at least
10,000 images, USB port for
connectivity to computer.
Should be able to operate
both on AC and battery.
Battery pack should be self-
recharging and should last at
least for 30 minutes or more
when fully charged.
Pg.79 Technical Specification (Pt.
no. 13)
Weight of the system may be specified
as mentioned in other portable item.
Additional point to specification
Amended
The system should be very
light with maximum of 7.5
kg. or less with internal
battery but without the
probes attached.
ITEM NO.8 (DIRECT DIGITAL FLAT PANEL FLUOROSCOPY & RADIOGRAPHY SYSTEM)
Pg.79 Technical Specification
Product Quality Standard:
Product may be USFDA and European
CE approved.
Should be USFDA/European
CE/BIS approved product. No Change
Pg.79 Technical Specification
Product Quality Standard:
The model should have AERB type
approved /NOC
The model should have AERB
type approved No Change
Pg.80 Technical Specification
All major components should be of
reputed make as most of the x-ray
equipment companies do not
manufacturer x-ray tube and detectors.
The most important factor is
compatibility of x-ray tube and detector
with the x-ray generator and carefully
managed exposure interlocks to avoid
any type of damage to the tube in case
of over load temperature and exposure
factors. Hence the point may be
deleted.
Or
Generator, Tube and flat panel
detector, out of three components, two
components should be from the main
manufacture
Generator & flat panel detector
should be from the main
manufacturer. In order to ensure
the quality of the equipment
Amended and Clarified as
The point “Generator & flat
panel detector should be
from the main manufacturer
in order to ensure the quality
of the equipment” is deleted
from the specification.
However, all the major
components of the system
such as generator, flat panel
detector, X-ray tube, Table,
Console, Control panel should
be clearly mentioned in the
AERB or CE certificate.
Relevant document should be
produced in the technical bid.
Pg.80 1.Table (Pt.no.1):
Floor mounted adjustable height table
with sliding table instead of floating top
of carbon fibre, scratch resistant
Floor mounted adjustable height
table with floating table top of
carbon fibre or equivalent suitable
scratch resistant surface
No Change
Page 10 of 49
surface should be provided.
Or
Height adjustment table may not be
required.
Pg.80 1.Table (Pt.no.5):
The typographical error may be
corrected as Motor Driven +90/- 45
degree or more table tilt along with
digital angle display.
Or
May be corrected as Motor Driven
+90/- 20 degree or more table tilt along
with digital angle display.
Or
May be corrected as Motor Driven
+90/- 90 degree or more table tilt along
with digital angle display.
Or
May be corrected as Motor Driven
+90/- 30 degree or more table tilt along
with digital angle display.
Motor Driven +900/- 450 degree
or more table tilt along with
digital angle display
Amended
Motor Driven +90/-20 degree
or more table tilt along with
digital angle display.
Pls specify the requirement of the
pressure injector with specification.
Injector interface (Additional
requirement to specification)
Amended
Pressure injector should be
provided with the system.
Pg.80 1.Table (Pt.no.1):
Single Digital flat panel Detector of size
35 x 43cm or more, made of
amorphous silicon with CSI scintillator.
Single Digital flat panel Detector
of size 43 x 43cm or more, made
of amorphous silicon with CSI
scintillator.
Amended
Single digital flat panel
Detector of size 35 x 43cm or
more made of amorphous
silicon with CSI scintillator.
Pg.80 1.Table (Pt.no.2):
Image Matrix 2688x2208 or better
Image Matrix 2800x2800 or
better
Amended
Image Matrix 2688x2208 or
better.
Pg.80 1.Table (Pt.no.8):
Patient Load: 200kg or more Patient Load: 160kg or more No Change
Pg.80 2.Digital Detector (Pt.no.3):
DQE >65% at may be 0.05lp/mm
instead of 0lp/mm.
Or
DQE>55 % at 0lp/mm
DQE>65 % at 0lp/mm
Amended
DQE >65% at should be
0.05lp/mm.
Pg.80 2.Digital Detector (Pt.no.5):
Digitization depth should be 16 bit
instead of 14bit.
Or
Digitization depth 12 bits or more
Digitization depth 14 bits or more No Change
Pg.80 2.Digital Detector (Pt.no.6):
Pixel size should be 160 micron or less.
Pixel size should be 150 micron or
less.
No Change
Page 11 of 49
Pg. 81 3.Monitors
Medical display should be 19”/21” LCD
for high –contrast (1.0/2.0 mega pixel)
Or
Display size may be 19inch or more
instead of 24inch.
Or
Medical grade 19” or more LCD
(1.0Mega pixel)
Medical grade 24” HD (2.0Mega
pixel)
Amended
Medical display should be
atleast 19inch or more LCD
for high contrast resolution of
minimum 1.0 mega pixel or
more.
Pg. 81 4.X-ray Generator Pt.1:
Radiography: mA range should be up to
1000mA.
mA Range: 10-1000mA
Amended
Radiography: mA range
should be up to 1000mA.
Pg. 81 4.X-ray Generator Pt.2:
The point may be deleted.
Touch screen operation for
multiprogramming. User defined
programs.
Amended
The point “Touch screen
operation for multi-
programming. User defined
programs” is deleted.
Pg. 81 4.X-ray Generator Pt.2:
Fluoroscopy: mA range: up to 20mA for
better fluoroscopy
mA range:0.5 to 5mA or better No Change
Pg. 81 4.X-ray Generator Pt.2:
Fluoroscopy
k v Range 50-125 kv or better
m A Range: 0.3 to 4mA or better
Fluoroscopy
(i) kv Range 40-110 kv or better
(ii) mA Range: 0.5 to 5mA or
better
No Change
Pg. 81 5.X-ray Tube (Pt.no.1)
One number dual focus x-ray tube
mounted on table stand with rotating
anode with 9000-10000rpm should be
provided.
Or
One number single couch mounted
Dual Focus X-ray tube with rotating
anode with 9000 rpm or more.
Or
X-ray tube for fluoroscopy should be
mounted in an over couch as all the
fluoroscopy system come with mounted
over couch
One number ceiling suspended
/Floor Mounted Dual Focus X-ray
tube with rotating anode with
9000 rpm or more
Amended
One number ceiling
suspended or Floor Mounted
or Couch mounted dual focus
X-ray tube with rotating
anode with 9000 rpm or
more.
Pg. 81 5.X-ray Tube (Pt.no.5)
Longitudinal movement 95cm or more
instead of 100cm or more.
Or
Longitudinal movement of tube across
the patient must be 90 cm or more.
Longitudinal movement of tube
across the patient must be 100
cm or more.
Amended
Longitudinal movement 90cm
or more.
Pg. 82 6.Direct Digital Imaging
System (Pt.no.1)
Field of view of at least 17inchX 14 inch
or more
Field of view of at least 40cms or
more No Change
Page 12 of 49
Pg. 82 6.Direct Digital Imaging
System (Pt.no.6)
Pulse fluoroscopy should be provided
with variable frame rate selection.
Additional point to specification No Change
Pg. 82 6.Direct Digital Imaging
System (Pt.no.7)
Trans lateral radiography may be
deleted.
Or
Vertical Bucky stand to perform
radiography may be added.
Provision for trans lateral
radiography should be available.
Amended
The point “Trans lateral
radiography” is deleted.
Pg. 82 7. Control Console, Image
Processing, Image display, Image
storage system and Transmission
Pt.5
System should have on line dosimeter
on the console to display actual
radiation dose or display on small
console.
System should have on line
dosimeter on the console to
display actual radiation dose.
Amended
System should have on line
dosimeter on the console to
display actual radiation dose
or display on small console.
Pg. 82 7. Control Console, Image
Processing, Image display, Image
storage system and Transmission
Pt.6
The feature may be optional feature.
Fully loaded Digital Subtraction
Angiography with all features.
Amended
The point” Fully loaded
Digital Subtraction
Angiography with all
features” is not mandatory.
Pg. 82 7. Control Console, Image
Processing, Image display, Image
storage system and Transmission
Pt.9
Multiple image display of 9 on 1 format.
Multiple image display of 16
images and 4 images.
Amended
Multiple image display of 9 or
more in one format.
Pg. 82 7. Control Console, Image
Processing, Image display, Image
storage system and Transmission
Pt.13
The point may be deleted.
Storage of fluoroscopic images
Amended
Storage of fluoroscopic
images is not mandatory.
Past performance in India/ Worldwide
should be allowed. In India Only No Change
ITEM NO.9 (FIXED X-RAY WITH MOTORIZED TABLE (600mA HIGH Frequency)
Pg.83 Product Quality Standard
Should be USFDA & European CE
approved model.
Or
Should be European CE / USFDA
approved model.
Should be USFDA/European CE/
BIS approved product No change
Pg.83 1. Generator (Pt. no.a)
Generator frequency may be 100kHz
instead of 200MHz or more.
Or
Generator should be high
frequency (200 MHz or more) for
constant output.
Amended
Generator should be high
frequency 100KHz or more
for constant output.
Page 13 of 49
Generator frequency may be 40Khz or
more.
Pg.83 1. Generator (Pt. no.f)
It should have automatic exposure
control device. Exposure time= 0.001
sec to less than 7second
It should have automatic
exposure control device exposure
time= 0.1 sec to less than
5second
Amended
It should have automatic
exposure control device.
Exposure time should be 0.1
sec to less than 7second.
Pg.84 2. X-ray Tube (Pt. no.e)
Tube with anode heat storage capacity
600 KHU or more instead of 300KHU or
more.
Tube with anode heat storage
capacity 300 KHU or more. No Change
ITEM NO.10 (C-ARM IMAGE INTENSIFIER)
Pg.85 1-X-ray Generator (Pt. no.2)
Power output may be 2.5KW or more.
Or
Power output: 3.5KW or more.
Power output: 6.0 KW or more
Amended
Power output: 2.5 KW or
more
Pg.85 2-Control (Pt. no.8)
mAs range should be 0.1 to 100mAs or
higher instead of 0.1 to 300mAs.
Or
Radio timer:0.1 to 200mAs in 20 steps
In built radio timer that enables
to select mAS from 0.1 to 300 in
25steps for radiography.
Amended
In built radio timer that
enables to select mAS from
0.1 to 200mAs or more in
20steps or more for
radiography.
Pg.85 2-Control (Pt. no.6)
Request for 25mA or more Radiography mA: 80mA or more No Change
Pg.85 3.X-ray Tube (Pt. no.1)
Anode type may be Stationary Anode
instead of rotating anode.
Rotating Anode
Amended
Anode should be stationary
or rotating type.
Pg.85 3.X-ray Tube (Pt. no.2)
Small Focal Spot:0.6mm and Large
focal spot: 1.0mm & heat storage
capacity:80KHU
Or
Small Focal Spot:0.6mm and Large
focal spot: 1.6mm. Anode heat storage
capacity:56KHU or more and tube
housing capacity: 1100KHU or more
Small focal spot:0.3mm (max.
Power:5kw) Large focal
spot:0.6mm (Max power :17KW)
Anode heat storage capacity
:250KHU or more
Amended
Small Focal Spot:0.6mm or
less and Large focal spot:
1.0mm or more. Anode heat
storage capacity: 56KHU or
more
Pg.86 4. CCD Camera
High resolution compact CCD camera
½‖ size. Total pixels: 1280(H) X
1024(V) should be there.
High resolution compact CCD
camera ½ inch size. Total pixels:
752(H) X 582(V) should be there.
No Change
Pg.86 5. Monitor
Monitor:27” or more with split screen
along with trolley
Two nos. 21” high resolution
monitors along with a trolley
Amended
Should have two nos. 21inch
or more high resolution
monitors or single monitor of
27inch or more with split
Page 14 of 49
screen provided along with a
trolley.
Pg.86 8. C-Arm Mobile Stand
Horizontal Travel 200mm. Horizontal Travel 210±10 mm No Change
Pg.86 9. Digital Image Memory
Systems:
Temp & Permanent storage up to
200images
Digital Image Memory Systems:
Temp & Permanent storage up to
100 frames
Amended
Temporary and Permanent
storage of 200 images or
more.
Pg.87 12. Quality Standard
Should be USFDA and European CE/BIS
approved product.
Should be USFDA/European
CE/BIS approved product. No Change
ITEM NO.12 (PORTABLE MOBILE X-RAY)
Pg.89 12. Pt.3
It should have powerful and rugged 4.0
kW high frequency (100KHz or more)
generators easy to plug to a standard
outlet 15AmP.
It should have powerful and
rugged 4.0 kW high frequency
generators easy to plug to a
standard outlet 15AmP.
No Change
Pg.90 Fixed Anode Tube
Focuses: 1.8mm or less Focuses: 0,6& 1,5 mm
Amended
Focuses: 1.8mm or less
Pg.90 Fixed Anode Tube
Exposure time: 10 ms to 5 s Exposure time: rom 1 ms to 10 s
Amended
Exposure time: 10ms to 5
sec. or more.
Pg.90 Fixed Anode Tube
The line has been repeated. May be
deleted.
Focal spot not more than 1mm.
Amended
The line “Focal spot not more
than 1mm” is deleted.
Pg.90 Product & Manufacturer
Quality Standards:
Should be USFDA and European CE/BIS
approved product.
Should be USFDA/ European
CE/BIS approved product. No Change
ITEM NO.13 (ANAESTHESIA WORKSTATION)
Pg.91 1. Gas Management
The system should be having an
integrated/modular Anaesthesia gas
module to measure inspired & expired
values of O2, N2O and all agents with
MAC value and should also display
these parameters with the CO2
waveform on the display of the
Anaesthesia Workstation.
Additional point to specification
Amended
The system should have an
integrated/modular
anaesthesia gas module to
measure inspired & expired
values of O2, Air or N2O and
all agents with MAC value
and should also display these
parameters with the CO2
waveform on the display of
the Anaesthesia Workstation.
Pg.91 1. Gas Management Pt.No.5
Electronic /mechanical Gas mixing
measurement and display od accurate
Electronic Gas Mixing
measurement and display for
accurate gas flows and mixing
No Change
Page 15 of 49
gas flow and mixing
Pg.91 1. Gas Management
Pt.No.11
The point should be deleted.
Should have decision support tool
for optimizing FGF No Change
Pg.91 1. Gas Management
Pt.No.14
Should be supplied from OEM of the
item.
Reusable adult and paediatric
autoclavable silicone circuit -
02nos. for each
No Change
Pg.91 1. Gas Management
Pt.No.19
Total agent consumption in ml should
be measured and displayed on the
screen.
Total agent consumption in ml
should be measured & displayed
on the screen, with a log of at
least 3 cases
No Change
Pg.91 1. Gas Management
Pt.No.21
Pause gas Flow (Preferable) – turns off
all gases for one minute during
intubation or suctioning / cardiac
bypass mode
Pause gas Flow (Preferable) –
turns off all gases for one minute
during intubation or suctioning
Amended
Pause gas flow: turns off all
gases for one minute during
intubation or suctioning or
cardiac bypass mode
Pg.91 1. Gas Management
Pt.No.19 to 21
The three points should be deleted.
• Total gas consumption for 02,
N20 or Air, to be measured and
displayed on the display screen
• Total Agent consumption in ml
should be measured and
displayed on the screen, with a
log of at-least 3 cases.
• Pause Gas flow (preferable)-
turns off all gases for one minute
during intubation or suctioning
(optional)
No Change
Pg.92 2. Vaporizer:
Vaporizer should be USFDA approved. Additional point to specification
Amended
The vaporiser being an
integrated part of the
anaesthesia system should
also have USFDA approval.
Pg.92 2. Vaporizer Pt.no.7:
Vaporizer should have extended
delivery range of 0-5vol%
Vaporizer should have extended
delivery range of 0-6vol%
Amended
Vaporizer should have
extended delivery range of 0
to 5vol.%
Pg.92 3. Breathing system Pt.no.2:
Total circuit volume shall not exceed 3L
in case of pneumatic driven system.
Total circuit volume shall not
exceed 2.7 L, including absorber
volume.
Amended
Total circuit volume shall not
exceed 3L in case of
pneumatic driven system.
Pg.92 3. Breathing system Pt.no.8:
Components coming in contact with
patient gas shall be disposable or
Components coming in contact
with patient gas shall be
Amended
Components coming in
contact with patient gas shall
Page 16 of 49
autoclavable except for ventilator part
including flow sensors. Ventilator with
flow sensor should be autoclavable.
disposable or autoclavable.
be disposable except flow
sensors.
Pg.92 3. Breathing system Pt.no.9:
FIO2 monitoring should be available &
should be paramagnetic.
FIO2 monitoring should be
available. No Change
Pg.92 3. Breathing system
The CO2 absorber should have bypass
facility.
Additional point No Change
Pg.92 4. Ventilation Pt.no. 1:
The workstation should have integrated
anaesthesia ventilator system and
screen size (TFT/LCD) of 15 inches
Or
The workstation should have integrated
anaesthesia ventilator system and
touch screen display of screen size
(TFT/LCD of 10” or more
Or
The workstation should have integrated
Anaesthesia Ventilator system and
screen size (TFT/LCD) of 15" with
touchscreen interface.
The workstation should have
integrated anaesthesia ventilator
system and screen size (TFT/LCD)
of 7 inches
Amended
The workstation should have
integrated anaesthesia
ventilator system and screen
size (TFT/LCD) of 10 inches
or more.
Pg.92 4. Ventilation Pt.no. 3:
Visible bellows for visual indication of
leak in the system or electronic alarm
for leakage in system to be displayed.
Visible bellows for visual
indication of leak in the systems
Amended
Visible bellows for visual
indication of leak in the
system or electronic alarm for
leakage in system to be
displayed.
Pg.92 4. Ventilation Pt.no. 4:
Delete dual mode and add SIMV/PS
Dual mode PCV, VCV and PS
needed for difficult lung
ventilation, Obese patient
laparoscopy, breathing heart and
neonatal
Amended
PCV, VCV and PS should
available for difficult lung
ventilation, obese patient
laparoscopy, breathing heart
and neonatal.
Pg.92 4. Ventilation Pt.no. 7:
Delete apnea back up
SIMV and pressure support
ventilation with apnea backup
ventilation should be offered
Amended
SIMV and pressure support
ventilation should be offered.
Pg.92 4. Ventilation Pt.no. 10:
The point should be deleted.
Or
The point should be retained.
Compliance measurement and
trending (Preferable): Measures
and displays the patients
compliance to offer an view of the
patient lung condition (lung
spirometry including PV and FV
loops)
Amended
Should have facility to
measure and display the
patient compliance for view
of the patient lung condition.
Pg.92 4. Ventilation Pt.no. 11:
Please remove the complete point from
the existing technical specification
Vital capacity & cycling
procedures (preferable): to
automate the procedure for
Amended
Should have lung recruitment
tool for optimal peep setting.
Page 17 of 49
Or
The point should be retained.
optimal peep setting to recruit the
lungs.
Pg.92 4. Ventilation Pt.no. 12:
Tidal volume: 20ml to 1400ml
Tidal volume: 20ml to 1500ml in
VCV, TV=minimum in PCV mode
Amended
Tidal volume should be 20ml
to 1400ml. or more in VCV,
TV=minimum in PCV mode
Pg.92 4. Ventilation Pt.no. 14:
Electronic PEEP: off 0-20 cmH2O
Electronic PEEP: Off ,4 to 20cms
H2O No Change
Pg.92 4. Ventilation Pt.no. 15:
Settable I:E ratio pause, Trigger (0.5-
10L/min). Insp pressure from 5 up to
50 cms H2O
Settable I:E ratio pause, Trigger
(0.2-10L/min). Insp. pressure
from 5 up to 50 cms H2O
Amended
Settable I:E ratio pause,
Trigger (0.5 to 10L/min).
Insp pressure from 5 up to
50 cms H2O.
Pg.92 4.Ventilation Pt.no. 23:
Machine should have mounting
capability of one O2 and one N2O pin-
index cylinder.
Machine should have mounting
capability of two O2 and two
N2O pin-index cylinder
Amended
Machine should have
mounting capability of two O2
and one N2O pin-index
cylinder.
Pg.94 5.Display Pt.no. 1:
12”colour display with USFDA
certification
Or
Around 15" Color TFT Touchscreen
Display with high visibility and highly
visible alarm light mounted on the
Anaesthesia Workstation
Around 15" Color TFT Display
with high visibility and highly
visible alarm light mounted on the
Anaesthesia Workstation.
Amended
Should have 12" or more
color TFT Display with high
visibility and highly visible
alarm light mounted on the
Anaesthesia Workstation.
Pg.94 5.Display Pt.no. 5:
Battery backup 3hrs.instead of 2hrs.
Should have an individual battery
backup minimum of 2hrs. No Change
Pg.94 5. Display Pt.no. 8:
Basic Patient side module for Measuring
Parameters like 5 lead ECG, NIBP, low
perfusion SPO2, RESP, 2xIBP, 2xTemp.
Additional modules to measure
parameters like level of Depth of
Anesthesia monitoring and NM
monitoring. EtCo2(side stream) with
Anesthesia Gas monitoring should be
offered as an option as the Anesthesia
Gas Module is to be supplied with
Anesthesia Workstation
Basic Patient side module for
Measuring Parameters like 5 lead
ECG, NIBP, SPO2,RESP,2xIBP,
2xTemp,EtCo2(side stream),
Anesthesia Gas monitoring, Level
of Depth of Anesthesia monitoring
and NM monitoring
Amended
Basic Patient side module
should be supplied for
measuring parameters like 5
lead ECG, NIBP, low
perfusion SPO2, RESP, 2xIBP,
2xTemp.
Should have additional
module for EtCO2(side
stream/main stream),
Anesthesia Gas monitoring,
Level of Depth of Anesthesia
monitoring and NM
monitoring.
Pg.94 Accessories Pt.no.1
Lead ECG Cable with diathermy
protection (2 Nos.)
Standard use for ECG (2 in no.)
No Change
Pg.94 Accessories Pt.no.6
NM monitoring cables recording option
EtCO2-10 filter assemblies and 10
tubing for anaesthesia gas
Amended
EtCO2-10 filter assemblies
Page 18 of 49
for printing up to 3 waveforms instead
of 4 waveforms and alphanumeric data,
and trends etc.
monitoring, depth of anaesthesia
monitoring (with 25 disposable
leads), NM monitoring cables,
recording option for printing up to
4 waveforms and alphanumeric
data, and trends etc.
and 10 tubing for anaesthesia
gas monitoring, depth of
anaesthesia monitoring (with
25 disposable leads), NM
monitoring cables, recording
option for printing of
minimum 3 waveforms and
alphanumeric data, and
trends etc.
Pg.94 Breaking Mechanism
The system should have a central
locking system.
Front caster wheel should have a
braking mechanism
Amended
The system should have a
central locking system.
Pg.95 Upgrades
The point should be deleted.
Facility of automatic electronic
charting solution with data
archival facility for patient
monitor and ventilator data. It
should be single centralized
server based for multiple beds
upgrade
Amended
The point “Facility of
automatic electronic charting
solution with data archival
facility for patient monitor
and ventilator data. It should
be single centralized server
based for multiple beds
upgrade” is deleted.
Pg.95 Quality standards
The anaesthesia Workstation \model
should be European CE approved and
patient monitor model should be both
USFDA and European CE approved
The anaesthesia Workstation and
patient monitor should USFDA
and European CE approved
No Change
Pg.95 Technical Specification (Pt.
no.-8 Up gradation)
The requirement of mentioned up
gradation should be clearly specified as
optional has been written.
Or
1.Mainstream/Side Stream/Mico Stream
EtCO2 monitoring should be possible.
3. Cardiac Output module for
measuring the cardiac output using the
thermo-dilution technique with total
four Invasive pressure channels in the
monitor.
5. SvO2/ScVO2 monitoring or similar
software with Calibration kit.
6. Facility for Mainstream/
Sidestream/Micro stream EtCO2 with
dedicated accessories for Adult,
Paediatric& Neonates (25 each) for
Sidestream and microstream and
atleast 5 reusable airway adapter each
for adult & for paediatric/neonatal
1. Mainstream EtCO2 monitoring
should be possible
2. EEG-minimum 4 channels with
display of spectra
3. Cardiac Output module for
measuring the cardiac output
using the thermo-dilution
technique with four Invasive
pressure channels
4. Module for monitoring Cardiac
Output
5. Facility for monitoring
transcutaneous O2 /CO2 and
ScVO2 monitoring or similar
software with Calibration kit
6. Facility for Micro stream EtCo2
with dedicated accessories for
Adult, Paediatric& Neonates
(25 each)
7. Facility of automatic electronic
charting solution with data
archival facility for patient
Amended
The patient monitor should
have facility for following
parameters and shall have to
be quoted accordingly.
1. EEG-minimum 4 channels
with display of spectra
2. Cardiac Output module or
provided with separate
standalone Cardiac Output
monitor for measuring the
cardiac output using the
thermo-dilution technique
with four invasive
pressure channels or
3. Facility for monitoring
transcutaneous O2 /CO2
and ScVO2 monitoring or
similar software with
Calibration kit.
4. Accessories for
Sidestream EtCo2 for
Page 19 of 49
patients. monitor and ventilator data. It
should be single centralized
server based for multiple beds
upgrade.
Adult, Paediatric (25 each)
ITEM NO.14 (MULTI PARA PATIENT MONITOR)
Quality Standard:
USFDA/CE approved by notified body
USFDA and European CE
approved No Change
Pg.95 Technical Specification (Pt.
no.-A Basic Monitor)
Monitor module for ECG, HR, RR, SPO2
and NIBP, IBP (Combined or separate
or integrated) and EtCO2, AGM and CO-
modular type with capability of
accepting atleast 2 modules.
Or
Monitor should be modular type, with
capability of accepting at least 4
modules/ smart module/Flexi port.
Or
All parameters should be
interchangeable between the monitors
without help of any service engineer.
Monitor should be modular type,
with capability of accepting at
least 4 modules.
Amended
Should be a modular monitor
with module for ECG, HR, RR,
SPO2 and NIBP (Combined or
separate or integrated) and
separate individual module
for 2 IBP, EtCO2, AGM and
Cardiac Output of modular
type with capability of
accepting atleast 4 modules.
All modules should be
interchangeable.
Pg.95 Technical Specification (Pt.
no.-A Basic Monitor Pt.2)
Display size may be atleast 15inch or
more instead of 12inch.
Or
Should have a minimum 12 inch TFT
color touch display screen or more
Should have a minimum 12 inch
TFT color display screen or more.
Amended
It should have a minimum 12
inch or more TFT color touch
display screen.
Pg.96 Technical Specification (Pt.
no.-A Basic Monitor Pt.7)
Should be capable of numerically
displaying information of all parameters
for which waveforms are being
displayed as well as displaying numeric
values of all additional modules
attached.
Should be capable of numerically
displaying information of all
parameters for which waveforms
are being displayed as well as
displaying numeric values of
additional parameters if more
than 4 modules are being used at
a time.
Amended
Should be capable of
numerically displaying
information of all parameters
for which waveforms are
being displayed as well as
displaying numeric values of
all additional modules
attached.
Pg.96 A. Basic Monitor Pt. no.3
Should be capable of displaying 120
hour trends for the monitored
parameters
Should be capable of displaying
24 hour trends for the monitored
parameters
Amended:
Should be capable of
displaying 72hour trends for
the monitored parameters.
Pg.96 A. Basic Monitor Pt. no.6
Should be able to display at least 10
waveforms or more with facility of over
lapping pressure waveform
Should be able to display at least
6 wave forms with facility of
overlapping pressure waveforms
No Change
Page 20 of 49
Pg.96 A. Basic Monitor Pt. no.8
Should have DICOM & HL7 facility
Should have DICOM facility and
connectivity to computer local
area network (LAN)(preferable)
Amended
Should have DICOM or HL7
facility and connectivity to
computer local area network.
Pg.96 B. Modules Pt. no.1)
ECG, Respiration SPO2, NIBP & Dual
Temp should be in a single module for
space saving
Or
Should be supplied with individual each
parameter module or smart flexi port
module to connect any parameter.
It should be possible for each
monitor accept modules
1.ECG+ Respiration: One
2.Oxygen saturation (pulse
Oxymeter/SpO2: One
3.Non-Invasive Blood Pressure
(NIBP): One
Temperature: Two
Amended
Should be a modular monitor
with module for ECG, HR, RR,
SPO2 and NIBP (Combined or
separate or integrated) and
separate individual module
for 2 IBP, EtCO2, AGM and
Cardiac Output of modular
type with capability of
accepting atleast 4 modules.
All modules should be
interchangeable.
Pg.96 Technical Specification (Pt.
no.-B Modules)
Under Oxygen saturation for pulse
Oxymeter, low perfusion and motion
condition functionality should be
mentioned.
Oxygen saturation (Pulse
Oxymeter/SpO2): One
Amended
Oxygen saturation (Pulse
Oxymeter/ SpO2): One
Should operate under low
perfusion and motion
tolerance condition and
should have either MASIMO
SET or NELLCOR OXIMAX
technology in the probe as
well as monitor.
Pg.96 B. Modules Pt. no.7
EtCO2 may be either side stream or
main stream or micro stream.
End-tidal CO2 monitoring (EtCO2)
Main stream: One
Amended
End-tidal CO2 monitoring
(EtCO2) Mainstream/ Side
stream: One
Pg.97 E. Pulse Oxymeter Pt. no.1
Should display plethysmograph and
Spo2 values with perfusion index also
Should display plethysmograph
and SpO2 values
Amended
Should display
plethysmograph and SpO2
values with perfusion index.
Pg.97 E. Pulse Oxymeter Pt. no.5
Adult & paediatric SpO2 Probes Adult or paediatric SpO2 Probes
Amended
Reusable adult or paediatric
probes (finger probes-2 nos.
and multisite-2 nos.) as
required should be provided
with each monitor
Pg.97 H. Cardiac Output Pt. no.1
May have Cardiac output monitoring:
one instead of Continuous cardiac
output monitoring: one
Or
Cardiac output of thermodilution
method may be allowed.
Continuous cardiac output
monitoring: one No Change
Page 21 of 49
Pg.97 J. End-tidal CO2 Pt. no.4
The point may be deleted.
Sampling tubes:10nos to be
provided with each module No Change
Pg.97 K. Printer Pt. no.1
Built in thermal printer should be
provided which should be able to print
data from monitor.
Single central printer should be
provided which should be able to
print data from selected monitor
Amended
Printing facility is not
required.
Pg.97 K. Printer Pt. no.3
Should be able to print real-time or
saved output of 2 channels.
Should be able to print real-time
or saved output of 3 channels
e.g. ECG and 2 invasive
pressures.
Amended
Printing facility is not
required.
Pg.98 L. AGM Module
AGM module: CO2:0-99mmHg instead
of 0 to 100mmHg.
CO2:0-100mmHg
Amended
AGM module: CO2: 0 to
99mmHg
Additional Specification: Monitor
should be upgradable to have
spirometer, non-invasive haemoglobin
and ScVo2 through interchangeable
modules.
Manufacturer should be capable to
upgrade ICU monitoring system to an
USFDA approved integrated clinical
information system with automated
charting of same make
Additional point to specification No Change
ITEM NO.15 (MULTI PARAMETER MONITOR WITH CENTRAL WORKSTATION)
Pg.99 A. Basic Monitor Pt. no.1
Monitor should be modular type with
capability of accepting at least 4
modules/ smart module
Or
All the modules of all parameters
should be interchangeable.
Or
Monitor should be modular type with
capability of accepting atleast 3
modules
Or
Monitor module for ECG, HR, RR, SPO2
and NIBP, IBP (Combined or separate
or integrated) and EtCO2 module with
Central workstation having capability of
atleast 2 modules.
Monitor should be modular type
with capability of accepting
atleast 4 modules
Amended
Should be a modular monitor
with module for ECG, HR, RR,
SPO2 and NIBP (Combined or
separate or integrated) and
separate individual module
for 2 IBP, EtCO2 and Cardiac
Output of modular type with
capability of accepting atleast
4 modules. All modules
should be interchangeable.
Pg.99 A. Basic Monitor Pt. no.2
It should have a minimum 17inch TFT
touch screen color Display screen or
more
Or
Should have a minimum 12inch TFT
It should have a minimum 12inch
TFT color display screen or more
Amended
Should have a minimum
12inch or more touch screen
color display screen.
Page 22 of 49
touch screen color display screen or
more
Pg.99 A. Basic Monitor Pt. no.3
Should be capable of displaying 120
hours trends for the monitored
parameters
Or
Should be capable of displaying
72hours trends with full disclosure for
the monitored parameters
Should be capable of displaying
24hour trends for the monitored
parameters
Amended
Should be capable of
displaying 72hour trends for
the monitored parameters
Pg.99 A. Basic Monitor Pt. no.6
Should be able to display at least 10
waveforms or more with facility of over
lapping pressure waveform
Or
Should be able to display at least 6
wave forms.
Should be able to display at least
6 wave forms with facility of
overlapping pressure waveforms
No Change
Pg.99 A. Basic Monitor Pt. no.7
Should be capable of numerically
displaying information of all parameters
for which waveforms are being
displayed, as well as displaying numeric
values of additional parameters if more
than 2 modules are being used at a
time.
Should be capable of numerically
displaying information of all
parameters for which waveforms
are being displayed, as well as
displaying numeric values of
additional parameters if more
than 4 modules are being used at
a time.
No Change
Pg.99 A. Basic Monitor Pt. no.8
Should have DICOM & HL7 facility
Or
Should have connectivity to computer
local area network (LAN) (preferable)
Should have DICOM facility and
connectivity to computer local
area network (LAN) (preferable)
Amended
Should have DICOM or HL7
facility and connectivity to
computer local area network.
Pg.99 B. Modules
It should be supply with individual each
parameter module or smart flexi port
module to connect any parameter
Modules: It should be possible for
each monitor to accept modules
No Change
Pg.99 B. Modules
ECG, Respiration SPo2, NIBP & Dual
Temp should be in a single module for
space saving
It should be possible for each
monitor accept modules
1.ECG+ Respiration: one
2.Oxygen saturation (pulse
Oxymeter/Spo2:one
3.Non-Invasive Blood Pressure
(NIBP):one
Temperature: Two
Amended
Should be a modular monitor
with module for ECG, HR, RR,
SPO2 and NIBP (Combined or
separate or integrated) and
separate individual module
for 2 IBP, EtCO2 and Cardiac
Output of modular type with
capability of accepting atleast
4 modules. All modules
should be interchangeable.
Pg.99 B. Modules pt. no. 6
Continuous /Thermo dilution Cardiac
Continuous Cardiac output
monitoring: One No Change
Page 23 of 49
output monitoring: One
Pg.100 E. Pulse Oxymeter Pt.no.1
Should display plethysmograph and
SpO2 values with perfusion index also
Should display plethysmograph
and Spo2 values
No Change
Should display
plethysmograph and SpO2
values with perfusion index.
Pg.100 E. Pulse Oxymeter Pt. no.5
Adult & paediatric SpO2 Probes Adult or paediatric SpO2 Probes
Amended
Reusable adult or paediatric
probes (finger probes-2 nos.
multisite-2 nos.) as required
should be provided with each
monitor.
Pg.101 J. End-Tidal CO2 Pt. no.1:
Side stream Monitoring of EtCO2 may
be allowed.
Or
Microstream may be asked.
Main stream Monitoring of CO2
Amended
End-tidal CO2 monitoring
(EtCO2) Mainstream/ Side
stream: One
Pg.101 J. End-Tidal CO2 Pt. no.2:
Display of pCO2 (mm Hg) and
concentration (%) may not be required.
End tidal CO2: Display of pCO2
(mmHg) and concentration (%)
Amended
The point “End tidal CO2:
Display of pCO2 (mmHg) and
concentration (%)” is
deleted.
Pg.101 J. End-tidal CO2 Pt. no.4
The point may be deleted.
Sampling tubes:10nos to be
provided with each module No Change
Pt.102 Central Monitoring Work
station- Product Quality Standard:
USFDA/CE approved by notified body
Or
Central Monitoring System (Japan) FDA
and CE approved
Or
Should be USFDA approved model.
USFDA and European CE
approved No Change
Pt.102 Central Monitoring Work
station:
Central Station Monitor of minimum 19
inch or more LED to be provided with
one laser printer and one minimum 19
inch slave monitor. All the monitors
should be connected via wired /
wireless. One CNS should be able to
connect up to 16 monitors.
Central Station Monitor of
minimum 21inch LED to be
provided with one laser printer
and one minimum 21inch slave
monitor. All the monitors should
be connected via wired / wireless.
One CNS should be able to
connect up to 30 monitors.
No Change
Pt.102 Central Monitoring Work
station:
Monitor should have the facility to
communicate bed to bed and bed to
Central without having a wired /
wireless network and the same shall
Monitor should have the facility to
communicate bed to bed and bed
to Central without having a wired
network and the same shall
provide the capability to control
and interact with remotely –
Amended
Monitor should have the
facility to communicate bed
to bed and bed to Central
with wired or wireless
network and the same shall
Page 24 of 49
provide the capability to control and
interact with remotely – viewed
parameters to maximize efficiency
viewed parameters to maximize
efficiency
provide the capability to
control and interact with
remotely viewed parameters
to maximize efficiency.
Pg.102 Central Monitoring
Workstation Pt. no.1
CNS should able to connect up to 16
monitors instead of 30 monitors.
One CNS should be able to
connect up to 30 monitors.
Amended
One CNS should be able to
connect up to 16 monitors.
Pg.102 Central Monitoring
Workstation Pt. no.6
Trend storage of CNS should be for
atleast 72hrs. instead of 24hrs.
Or
CNC should have 150 hr. stored patient
data monitoring –trends (pre & post
discharge both)
CNC should have 150 hr. event review
facility
CNS should offer wave review with 150
hr. full disclosure
CNS should have 24 hr stored
patient data monitoring – trends
Amended
CNS should have atleast 72
hrs. or more stored patient
data monitoring trends.
ITEM NO.16 (VENTILATOR)
Under Quality standard
The model should be US FDA or
European CE approved
Or
Should retain USFDA and European CE
approved.
The model should be US FDA and
European CE approved No change
Pg.103 Technical Specification (Pt.
no.2)
Microprocessor Controlled suitable for
Neonate to Adult ventilation
Microprocessor Controlled suitable
for paediatric to Adult ventilation
Amended
Microprocessor controlled
suitable for infant to Adult
ventilation.
Pg.103 Technical Specification (Pt.
no.4)
Should have built in touch color screen
TFT display of minimum 10” or more for
display of waveforms and monitored
value.
Or
Screen should be 15 inch or more for
display of waveforms and monitored
value.
Should have built in touch color
screen TFT display of minimum
12” or more for display of
waveforms and monitored value
No change
Pg.103 Technical Specification (Pt.
no.5)
EtCO2 facility may be integrated instead
of inbuilt in the ventilator.
Should have inbuilt facility to
upgrade with EtcO2. No Change
Page 25 of 49
Pg.103 Technical Specification (Pt.
no.7)
Should have automatic compliance and
leakage compensation for circuit up to
100L/Min
Automatic compliance and
leakage compensation circuit No Change
Pg.103 Technical Specification (Pt.
no.9(a)
Tidal volume should be minimum of
50ml to 2000ml.
Or
2ml Tidal Volume onwards to cover
entire range
Or
Tidal Volume:5ml to 2000ml
Tidal volume (Minimum at least
20ml, Maximum up to 2000ml) No Change
Pg.103 Technical Specification (Pt.
no.9 .b)
Inspiratory pressure (up to 60cm of
H2O or more
Or
Inspiratory pressure :0-100cmH2o for
efficient ventilation
Inspiratory pressure (up to 80cm
of H2O or more
No Change
Pg.103 Technical Specification (Pt.
no.9.c)
Respiratory should be 5 to150bpm
Respiratory should be 1-80 bpm
Amended
Respiratory should be 5 to 80
bpm
Pg.103 Technical Specification (Pt.
no.9 (i)
Pressure or Flow Trigger
Pressure and Flow Trigger No Change
Pg.103 Technical Specification (Pt.
no.9 (j)
Inspiratory flow up to 210lpm
Inspiratory flow upto 180lpm No Change
Pg.103 Technical Specification (Pt.
no.9 (l)
Volume trap may be included.
Occlusion pressure No Change
Pg.104 Technical Specification (Pt.
no.10)
The lung recruitment or lungs
protection tools software may be asked.
Additional feature
Amended
The advanced modes and
lung recruitment or lungs
protection tools software
should be provided.
Pg.104 Technical Specification (Pt.
no.11)
Request to add –ATC should be
available as a weaning parameter
Or
Newer modes like lungs protective
modes: PRVC. APRV,
Bilevel/BiVent/DuoPAP
Waning modes: Volume
Should have facility for invasive
and non-invasive ventilation No Change
Page 26 of 49
support/Spontaneous breathing
trial/NAVA
Closed loop ventilations: ASV/Smartcare
PS/BiLevel-VG/Automode
Pg.104 Technical Specification (Pt.
no.11(h))
Dedicated NIV mode should be
available.
Non-invasive ventilation in all
modes (BIPAP, CPAP) No Change
Pg.104 Technical Specification (Pt.
no.11(j))
Request to add inverse ratio ventilation
/APRV
Inverse ratio ventilation
Amended
Inverse ratio ventilation/
APRV (Airway pressure
release ventilation)
Pg.104 Technical Specification (Pt.
no.12)
Should have built in safety alarms for
Airway Pressure High & Low, Minute
Volume High & Low ,Power Failure, Low
Oxygen ,High respiratory Rate, Air
Source in – operable/Low pressure
Should have built in safety alarms
for Airway Pressure High & Low,
Minute Volume High & Low
,Power Failure, Low Oxygen ,High
respiratory Rate, Air Source in –
operable
No Change
Pg.104 Technical Specification (Pt.
no.13)
Inbuilt exhalation filter may be deleted
and detachable autoclavable expiratory
block may be added.
Or
Atleast 100 disposable exhalation filters
should be provided.
Should have inbuilt exhalation
filter
Amended
Should have inbuilt
exhalation filter or detachable
autoclavable expiratory block.
In case of exhalation filter,
100 pcs. Should be supplied
with the system.
Pg.104 Technical Specification (Pt.
no.14)
Turbine system may be allowed.
Or
The ventilator should be inbuilt turbine
driven with peak flow of 260L/Min or
more
Or
Ventilator should be Compressor
/Turbine driven and from the same
manufacturer
Or
Ventilator should be compressor driven.
Ventilator should be compressor
driven and should be of same
manufacturer
No Change
Pg.104 Technical Specification (Pt.
no.16-For humidifier)
USFDA/CE approved by notified body
USFDA and European CE
approved No Change
Pg.104 Technical Specification (Pt.
no.16-For humidifier)
Humidifier should be supplied with
proximal sensor & its warranty should
be cover up to warranty period of
Additional point to specification
Amended
Humidifier should be supplied
with proximal sensor & its
warranty should be cover up
to warranty period of
Page 27 of 49
ventilator ventilator.
It should be from OEM Hinged arm holder for holding the
circuit No Change
Pg.104 Technical Specification (Pt.
no.17)
Inbuilt nebulizer for better synchrony
with particle size less than 3 micron.
Or
Nebulization assembly compatible with
ventilator and circuit, inspiration
synchronised and particle size less than
0.3micron.
Nebulization Technology should be
ultrasonic or vibrating mesh. The
nebulizer should also have USFDA & CE
quality certificate
Nebulization assembly compatible
with ventilator and circuit
,inspiration synchronized and
particle size less than 5 micron
No Change
Pg.105 Technical Specification (Pt.
no.20)
Expiratory cassette or valve unit life
should be more than warranty period of
the machine
Expiratory unit life should be
more than 3years
Amended
Expiratory cassette or valve
unit, flow sensors and
oxygen sensors should be
covered under warranty of
the system and must be
replaced free of cost within
the warranty period.
Pg.105 Technical Specification (Pt.
no.21)
Data storage facility for at least 7days
or more
Or
Data storage facility minimum 72 hrs.
Data storage facility for at least
24hrs or more
Amended
The trend data should be
available for atleast 48 hours.
Pg.105 Technical Specification (Pt.
no.22)
Internal battery: 4-6 hours of battery
can be helpful anytime & is available
(including inbuilt air source.
Internal rechargeable battery at
least 60 min backup. No Change
Pg.105 Technical Specification (Pt.
no.23)
Flow sensors and oxygen sensors if
required during the warranty period,
company will be supplied free of cost as
& when required.
Should have flow sensors and
oxygen sensors having long life
and the company shall specify the
lifecycle and the cost of the flow
sensors and oxygen sensors at
the time of quoting the tender
Amended
Flow sensors and oxygen
sensors shall be supplied free
of cost by the supplier during
the warranty period.
Pg.105 Technical Specification (Pt.
no.24.b)
It should be from OEM
• Non-invasive ventilator masks
reusable for adult (3 sizes) and
paediatric according to age 4 sets
each
• HME filter-50nos.
Amended
The following items should
be from OEM with having
product catalogue number
• Non-invasive ventilator masks
Page 28 of 49
• Disposable circuit-50no. reusable for adult (3 sizes)
and paediatric according to
age 4 sets each
• HME filter-50nos.
Disposable circuit-50no.
Additional Specification
Automatic Rise time: Automatic rise
time setting avoids pressure overshoots
follows patient breathing pattern and
adjusting rise time automatically. This
features is now available in addition to
conventional annual rise time setting.
So clinicians has a choice to manual rise
time or auto rise time
Additional point to specification No Change
Additional Specification
Automatic exhalation sensitivity. In
addition to conventional manual
exhalation trigger sensitivity now
automatic expiratory trigger sensitivity
is available. It allows better
synchronization as ventilator adjust
automatically exhalation sensitivity
based on patient breathing pattern for
spontaneously breathing patient. So
clinician has a choice to choose from
manual exhalation or automatic
exhalation trigger sensitivity.
Additional point to specification No Change
Additional Specification
Automatic leakage compensation upto
100L/min (compared to 40l/min or
60l/min)
For success of non-invasive ventilation
Automatic leakage compensation of
upto 100L/min or more peak, flow rate
above 200L/min & Automation of Rise
Time & Exhalation sensitivity are
important criterion .We strongly
recommend higher leakage
compensation upto 100L /min which
will impact success of non invasive
ventilation.
Additional point to specification No Change
Additional Specification
High Flow oxygen Therapy: Is widely
used now and is available with most
ventilator manufacturer. Possibly to
nebulization through high flow is also
available
Additional point to specification No Change
Page 29 of 49
Additional Specification
Lung Recruitment Tool: Automatic LRT
is now available & is extremely useful
for ATDS patient
Additional point to specification No Change
ITEM NO.17 (TRANSPORT VENTILATOR)
Under Quality standard
The model should be US FDA or
European CE approved
The model should be US FDA and
European CE approved No change
Pg.105 Technical Specification
Under product quality standard, shock
proof and vibration proof certificate
should be asked for the product.
Additional point
Amended
Test reports towards shock
proof and vibration proof of
the quoted model from
accredited testing laboratory
should be furnished in the
technical bid.
Pg.105 Product Quality Standard:
The USFDA approval should specify the
ventilator model for both intra hospital
and inter /pre hospital transport
purpose for both paediatric and adult
patient with invasive as well as non-
invasive ventilation modes under
indication of use. Devices with only
generic classification as portable
/transport would be summarily rejected.
Should be USFDA and European
CE approved model. CE certificate
must be furnished by notified
agency
Amended
The model should be certified
or approved as a transport
ventilator for both paediatric
and adult patients and it
should be approved for both
intra hospital and inter /pre
hospital transport purpose
and should support for air
ambulance use.
Pg.105 Technical Specification Pt.
no. 1
Mountable transport ventilator suitable
for neonatal to adult patient
Mountable transport ventilator
suitable for paediatric to adult
patients
No Change
Pg.105 Technical Specification Pt.
no. 3
Microprocessor/ Pneumatic controlled
Microprocessor controlled No Change
Pg.105 Technical Specification Pt.
no. 4
Delete PRVC and BiPAP and request to
add CPR mode and NIV
Or
Should have following modes of
ventilation: Assist control (pressure
controlled and volume controlled) CMV,
PS, SIMV and CPAP in both Invasive
and Non-Invasive type of ventilation
Or
CPAP can be eliminated.
Should have following modes of
ventilation: Assist control
(pressure controlled and volume
controlled) CMV, PS, SIMV and
CPAP, PRVC (CMV & SIMV)
No Change
Pg.105 Technical Specification Pt.
no. 5
Display 4”or more or 6” or more
Display 8” or more
Amended
Should have inbuilt user
interface display should be 6
inch or more.
Page 30 of 49
Pg.105 Technical Specification Pt.
no. 9
Tidal volume 50 to 2500ml.
Or
Tidal Volume 5ml -2000ml.
Or
Tidal volume range 50 to 1500 ml
Tidal volume range 30 to 1500 ml No Change
Pg.105 Technical Specification Pt.
no. 9
PEEP 0 to 20cm water
PEEP 0 to 30cm of water Amended
PEEP 0 to 20cm water
Pg.105 Technical Specification Pt.
no. 10
FiO2 setting range between 21% to
100% should be seamlessly selectable
at any value as per the application
requirement.
Any fixed setting between 21% to
100% wont be acceptable.
If the device is expected to work on low
pressure oxygen source like oxygen
concentrators or flow meters then
please specifically mention that the
device should provide oxygen
enrichment on both low (up to 10psi
like flow meter/ oxygen concentrator)/
high –pressure (40 to 60 psi) oxygen
supply source.
FiO2 setting range between 21%
to 100 % setting 100% FiO2
should be mandatory
Amended
FiO2 setting range between
21% to 100% should be
seamlessly selectable at any
value as per the application
requirement.
Any fixed setting between
21% to 100% shall not be
acceptable.
Pg.106 Technical Specification Pt.
no. 11(ii)
Flow triggers 3-15L/min
Flow triggers 1-10L/min No Change
Pg.106 Technical Specification Pt.
no. 12
Both flow and pressure trigger
Trigger sensitivity -Flow Amended
Both flow & Pressure Trigger
Pg.106 Technical Specification Pt.
no. 2.4
USB and Bluetooth connectivity
Software and /or standard of
communication (where ever
required)
No Change
Pg.106 Technical Specification Pt.
no. 4.2
Battery backup minimum 6hours
Should be both main and battery
operated with minimum battery
backup of 4 hrs.
No Change
Pg.106 Technical Specification Pt.
no. 5 (Accessories)
All from OEM
Pole mounting bracket
Adult test lung
Infant test lung
Amended
The following accessories/
consumables should be from
manufacturer approved OEM
supplier having product
catalogue number. Such as
Pole mounting bracket, Adult
test lung, Infant test lung.
Page 31 of 49
ITEM NO.18 (MULTIPARA MONITOR)
Pg.106 Quality Standard
USFDA/CE approved by notified body
USFDA and European CE
approved No Change
Pg.107 A)Basic Monitor Pt. no. 1
Monitor should be modular type, with
capability of accepting at least 4
modules. All parameters should be
interchangeable between the monitors
without help of any service engineer
Or
Monitor should be modular type with
capability of accepting atleast 3
modules instead of 4 modules.
Monitor should be modular type
with capability of accepting
atleast 4 modules
Amended
Should be a modular monitor
with module for ECG, HR, RR,
SPO2 and NIBP (Combined or
separate or integrated) and
separate individual module
for 2 IBP, EtCO2 and Cardiac
Output of modular type with
capability of accepting atleast
4 modules. All modules
should be interchangeable.
Pg.107 A)Basic Monitor Pt. no. 2
It should have a minimum 17 inch TFT
touch screen color Display screen or
more
It should have a minimum 12 inch
TFT touch screen color Display
screen or more
No Change
Pg.107 A)Basic Monitor Pt. no. 3
Should be capable of displaying 120
hour trends for the monitored
parameters
Or
96-hours graphic and tabular trends of
all parameters
Should be capable of displaying
24 hours trends for the monitored
parameters
Amended
Should be capable of
displaying minimum 72hour
trends for the monitored
parameters.
Pg.107 A)Basic Monitor Pt. no. 8
Should have connectivity to computer
local area network (LAN) - (preferable).
Should have DICOM facility and
connectivity to computer local
area network (LAN) -
(preferable).
No Change
Pg.107 B)Modules Pt. no. 3
ECG, Respiration, SPO2,NIBP & Dual
Temp should be in a single module for
space saving
It should be possible for each
monitor accept modules
1.ECG+ Respiration: one
2.Oxygen saturation (pulse
Oxymeter/Spo2:one
3.Non-Invasive Blood Pressure
(NIBP):one
Temperature: Two
No Change
Pg.107 B)Modules Pt. no. 6
Continuous /Thermo dilution Cardiac
output monitoring: One
Continuous Cardiac output
monitoring: One No Change
Pg.107 B)Modules Pt. no. 7
Microstream may be allowed.
Or
Sidestream EtCO2 should be allowed.
End-tidal CO2 monitoring (EtCO2)
Main stream: One
Amended
End-tidal CO2 monitoring
(EtCO2) should be main
stream/ sidestream: One
Pg.108 E)Pulse Oxymeter Pt. no. 7
Oxygen saturation Masimo SET with PVI
It should be capable of measuring
SPO2 in low perfusion status and
motion tolerance certification in
No Change
Page 32 of 49
this regard is to be attached.
Pg.108 H)Cardiac Output Pt. no. 1
Cardiac output monitoring: one
Or
Continuous /Thermo dilution Cardiac
output monitoring
Continuous cardiac output
monitoring: one No Change
Pg.110 K)Printer Pt. no. 1
Built in thermal printer should be
provided which should be able to print
data from monitor
Single central printer should be
provided which should be able to
print data from selected monitor
Amended
Printing facility not required.
Additional Specification:
Monitor should be upgradable to have
spirometry, non-invasive haemoglobin
and ScVo2 through interchangeable
modules
Manufacturer should be capable to
upgrade ICU monitoring system to an
USFDA approved integrated clinical
information system with automated
charting of same make
Additional point to specification No Change
19.MULTIPARA METER MONITOR (ECG, HR, RR, SPO2 AND NIBP)
Pg.110 Technical Specification
(Quality Standard)
USFDA/CE approved by notified body
USFDA and European CE
approved No Change
Pg.110 Technical Specification
Should be upgradable to ETCO2,IBP and
should be in form of external modules
which can be replaced easily
Standard Parameter No Change
Pg.110 Technical Specification
ECG:
Should have following software’s
ST Mapping, QT analysis, HRV analysis
Additional point to specification No Change
Pg.110 Technical Specification
SpO2:
From MASIMO
Or
MASIMO with PVI
Spo2 technology
Amended
SpO2 technology should work
and measure on low
perfusion condition and
motion tolerance.
Pg.110 Technical Specification
SpO2:
Should have storage facility of trends
on USB
72 hours graphic and tabular
trends of all parameter No Change
Pg.111 Technical Specification
Pulse Rate:
15” color LCD/TFT
Or
12inch colour touch LCD with high-
12inch colour LCD with high-
resolution displays patient
parameter.
Amended
Should have 12inch colour
touch LCD with high-
resolution displays patient
parameter.
Page 33 of 49
resolution displays patient parameter.
Additional: Monitor should be
upgradable to ETCO2, Minimal invasive
continuous cardiac output and 3IBP
through interchangeable modules
Manufacturer should be capable to
upgrade ICU monitoring system to an
USFDA approved integrated clinical
information system with automated
charting of same make
Additional point to specification No Change
ITEM NO.20 (DEFIBRILLATOR WITH & WITHOUT PACE MAKER)
Pg.111 Product Quality Standard:
The model should be US FDA or
European CE approved model. CE
certificate must be furnished by notified
agency
Should be USFDA and European
CE approved model certificate
must be furnished by notified
agency
No change
Pg.111 Technical Characteristics
Pt. no.1:
Biphasic waveform with 200Joules
Truncated dual phase exponential
wave form with charge of 1 to
360joules with operating
instructions on the panel of bi-
phasic defibrillator monitor or any
other energy configuration
desired by the user
No Change
Pg.111 Technical Characteristics
Pt. no.2:
With the equipment powered by electric
grid or even powered by the new
battery (and fully charged) its charge
time of up to 6 seconds to reach
maximum energy.
With the equipment powered by
electric grid or even powered by
the new battery (and fully
charged) its charge time from
maximum energy of up to 5
seconds for 200 joules or up to 6
seconds or 360 joules.
No Change
Pg.111 Technical Characteristics
Pt. no.10:
Capacity to perform minimum 100
discharges of 360 Joules with full load
(new battery fully charged)
Or
Should perform atleast 100 discharges
Capacity to perform minimum 220
discharges with full load (new
battery fully charged)
Amended
Should have capacity to
perform minimum 100
discharges with full load on
fully charged battery.
Pg.112 Technical Characteristics
Pt. no.11:
More details may be given.
External reserve batteries with
internal charger (Optional)
Amended
External reserve batteries
with internal charger not
mandatory.
Pg.112 Technical Characteristics
Pt. no.13:
Up to 1000 event memory and Up to for
24 hours consecutive ECG Waveform
Or
Event memory including curve,
date and hour, of approximately
250 MB that corresponds to over
100 hours of continuous
recording.
Amended
Event memory including
curve, date and hour of
atleast 100 events or up to
24 hours.
Page 34 of 49
100event memory including curve date
and hour
Pg.112 Technical Characteristics
Pt. no.17:
The communication should be done
with help of USB
Or
The point should be deleted.
Enable communication with micro
computer through connection for
memory data visualization
Amended
Communication facility should
be available through USB or
internal memory.
Pg.112 Technical Characteristics
Pt. no.22:
The above points may be removed.
When BIPHASIC DEFIBRILLATOR
is configured in automatic mode,
the change energy follows a
trigger of 150J and 200J.
No Change
Pg.112 Technical Characteristics
Pt. no.24:
Impedance detection in the 20 ohm to
200Ohm range for the triggering
Impedance detection in the 25
ohm to 500Ohm range for the
triggering
Amended
Impedance detection in the
25 ohm to 200Ohm range for
the triggering
Pg.112 Technical Characteristics
Pt. no.25,26,27:
The above points may be removed.
Software for drug calculation
Software for ventilation/
incubation mode
ST segment and arrhythmia
analysis
Telemetry software
Amended
The following points, such as
• Software for drug calculation
• Software for ventilation/
incubation mode
• ST segment and arrhythmia
analysis
• Telemetry software
is deleted from the
specification.
Pg.112 Technical Characteristics
Pt. no.29:
Memory data card for recording up to
for 24 hours Consecutive ECG
Waveform
Memory data card of 250MB that
correspond to over 100 hours of
continuous recording.
Amended
Memory data card for
recording up to for 24 hours
Consecutive ECG Waveform
should be available.
Pg.112 Technical Characteristics
Under Point ECG Characteristic,
Pt.2
12 derivations with 10 –lead ECG Cable
12 derivations for 5 way ECG
cable
Amended
12 derivations for 5 or 10
lead ECG cable.
Pg.112 Technical Characteristics
Under Point ECG Characteristic,
Pt.4
Cardiac Frequency : Any frequency
reading frequency from 10 to 150 rpm
with numerical presentation
Cardiac Frequency: Any frequency
reading frequency from 10 to 350
rpm with numerical presentation
Amended
Cardiac Frequency: Any
frequency reading frequency
from 10 to 150 Hz with
numerical presentation.
ITEM NO.21 (VIDEO BRONCHOSCOPE WITH PROCESSOR)
Page No 113 point A2
Distal End diameter maximum 0f
6.4mm
Distal End diameter maximum of
6mm or less
Amended
Distal End diameter
maximum 0f 6.4mm
Page 35 of 49
Page No 113 point A3
Insertion tube diameter of 6.4 mm or
less
Insertion tube diameter of 6mm
or less
Amended:
Insertion tube diameter of
6.4 mm or less
Page No 113 point A6
Should have 180 degree upward and
120 degree down ward deflection or
better
Should have 180 degree upward
and 120 degree down ward
deflection
No change
Page No 114 point A10
It should have xenon light source
It should have portable self-
illuminating white LED light
source light source
Amended
It should have LED/Xenon
light source
Page No 114 point C2.
HD processor system should have
xenon light source
HD processor system with 16: 9
aspect ratio with inbuilt LED light
sources
Amended
HD processor system with
16: 9 aspect ratios with
LED/Xenon light sources
Page No 114 point C7.
This should be removed as
recommended amendment is for xenon
light source
LED as a source of lamp with a
minimum color temperature of
5000K and minimum lamp life
hour 20000
Amended
LED/Xenon as a source of
lamp with a minimum color
temperature of 5000K
Page No 114 point C12
HDTV should be removed Video signal :
standards output :RGB, y/C composite
,DVI
Video signal: standards output:
HDTV: RGB, y/C composite ,DVI
Amended
Video signal: standards
output: RGB, y/C composite,
DVI
ITEM NO.22 (FLASH STERILIZER)
Page No 115 Quality Standards
Should be USFDA /CE (European origin)
approved product.
Should be USFDA and CE
(notified) approved product.
Amended
Should be USFDA or CE
(issued by notified European
agency) approved product.
Page No 115 Quality Standards
The IEC 60601 may be removed.
IEC 60601(or equivalent BIS
standard) No Change
Page No 115 Quality Standards
The EMC standard may be removed.
EMC for electro medical
equipment :61326-1
Amended
EMC for electro medical
equipment :61326-1 is not
mandatory.
Page No 116 Technical
Specification Pt.no.6:
The sterilization chamber /jacket and
steam generator should be made of
high quality stainless steel of 304L
/316L grades
The sterilization chamber, jacket
and steam generator should be
made of high quality stainless
steel of 316L grades
Amended
The sterilization chamber,
jacket and steam generator
should be made of high
quality stainless steel of 316
or 316L grades.
Page No 116 Technical
Specification Pt.no.7:
If required, should have an integrated
water purification system.
It should have an integrated
water purification system.
Amended
System should be provided
with integrated or separate
water purification system of
suitable capacity required for
one cycle of the sterilisation.
Page 36 of 49
Page No 116 Technical
Specification Pt.no.10:
The system should have safety features
for overheating of chamber / jacket
operation of the steam generator
without water
The system should have safety
features for overheating of
chamber, jacket operation of the
steam generator without water
Amended
The system should have
safety features for
overheating of chamber /
jacket operation of the steam
generator without water.
ITEM NO.23 (ETO MACHINE)
Page No 116 Technical
Specification Pt.no.1:
The depth of the sterilizer should be 60
inches instead of 36 inches. As the
catheters and long in some cases
Chamber size:16” x 16”x 36” No Change
Page No 116 Technical
Specification Pt.no.1:
Chamber material made of aluminium
sheet as it is better conductor than
stainless steel
Or
The Chamber should be Single /Double
walled made of suitable Material
(S.S.316L) which is Resistant to
corrosion and gas
Chamber should be double walled
made of SS316 grade.
Amended
The chamber should be
double walled made of
suitable material (SS 316 or
SS 316L) which is resistant to
corrosion and gas.
Page No 117 Technical
Specification Pt.no.4:
Better uniformity of temperature
heating should be done by hot water
circulating system.
There should be provision of
heating the chamber either with
strip air heater or hot water
circulated through a coil around
the chamber to maintain the
chamber temperature around 30
to 55 degree centigrade.
No Change
Page No 117 Technical
Specification Pt.no.8:
The sterilizer shall be provided with
suitable vacuum pump and gas trap (if
required) to separate and evacuate the
gas.
The sterilizer shall be provided
with suitable vacuum pump and
gas trap to separate and evacuate
the gas.
Amended
The sterilizer shall be
provided with either suitable
vacuum pump or gas trap to
separate and evacuate the
Gas or be provided with
exhaust pipeline system to
the atleast 25ft. above of the
system.
Page No 117 Technical
Specification Pt.no.9:
Vacuum pump should be diaphragm
only
Vacuum pump should be
diaphragm /water ring type No Change
Page No 117 Technical
Specification Pt.no.10.D:
Delete the point i.e. There should be
inbuilt gas catalytic converter for the
exhausted ETO gas.
There should be inbuilt gas
catalytic converter for the
exhausted ETO gas.
Amended
The point “There should be
inbuilt gas catalytic converter
for the exhausted ETO gas” is
deleted.
Page 37 of 49
Page No 117 Technical
Specification Pt.no.10.E(c):
Cartridge Puncturing /gas purging
should be automatic
Cartridge Puncturing /gas purging
depending on the cycle selected.
Amended
Cartridge puncturing or gas
purging should be automatic
depending on the cycle
selected.
Page No 117 Technical
Specification Pt.no.17:
Should be USFDA/CE certified.
Should Be USFDA And European
CE Certified. (Or equivalent)
Amended
Should be USFDA or CE
(issued by notified European
agency) approved product.
ITEM NO.24 (INSTRUMENT WASHER DISINFECTOR WITH TROLLEY)
Page No 119 2. Technical
Characteristics Pt.no.2.1:
The chamber should be single /double
walled made of suitable material
(s.s316L) which is resistant to corrosion
and gas
Double wall construction with
high quality insulation.
Amended
Should be double wall
construction with high quality
insulation and made of
suitable material (SS 316/SS
316L) resistant to corrosion
and gas.
Page No 120 3. Physical
Characteristics Pt.no.3.3:
The size mentioned in 50 to 60 liters
which is very small for CSSD
department. It should be from 300 to
500 liters.
The size mentioned in 50 to 60
liters No Change
Battery backup for display system by
UPS Additional point to specification No Change
ITEM NO.25(HORIZONTAL AUTOCLAVE)
Page No 122 2. Technical
Characteristics Pt.no.5:
It should have celling with only silicone
long lasting and durable gasket
Sealed with Neoprene/ Silicone
long-lasting and durable gasket.
Amended
Sealed silicone long-lasting
and durable gasket.
Battery with UPS is again advisable for
display system Additional point to specification No Change
Page No 122 4. Energy Source
Pt.no.4.7:
Power consumption 18KW
Power consumption: 18- 20kW No Change
ITEM NO.26(ULTRASOINC CLEANER)
Page No 125 Technical
Specification Pt.no. (v):
The capacity should not be less than 20
liters.
Should have a tank capacity of
minimum 10 L.
No change
ITEM NO.28(ABG MCHINE WITH ELECTROLYTE (CATRIDGE BASED)
Page No 126 Technical
Specification Pt.no. 7:
Should calculate analyte Hct.
Should measure analyte Hct. No Change
Page 38 of 49
Page No 126 Technical
Specification Pt.no. 8:
Should measure analyte tHb.
Should calculate analyte tHb.
Amended
Should be under measured
analyte for tHb.
Page No 126 Technical
Specification Pt.no. 9:
The point should calculate analyte
glucose may be deleted.
Should calculate analyte Glucose.
Amended
Glucose should be under
measured parameters.
Page No 126 Technical
Specification Pt.no. 10:
Should measure lactate
Should calculate lactate
Amended
Lactate should be under
measured parameters.
Page No 126 Technical
Specification Pt.no. 11:
Should measure Cl-.
Or
The point should calculate analyte Cl-
may be deleted.
Should calculate Cl-
Amended
Cl- parameter should be
under measured parameters.
Page No 126 Technical
Specification Pt.no. 13:
Software includes printouts of Levey –
Jenning /Static graph charts for quality
Software includes printouts of
Levey-jenning Charts for quality
Amended
Software includes printouts of
Levey –Jenning /Static graph
charts for quality.
Page No 126 Technical
Specification Pt.no. 14:
Method to recalibrate in current
environment not OEM factory calibrated
/Auto save current calibration, Auto
aspiration sample ,backlit display with
easy viewing in all ambient light levels
cartridges –combination of various
tests: Single cartridge/multiple test
cartridges
Method of recalibration /Save
current calibration, set sample
size Backlit display with easy
viewing in all display with easy
viewing in all ambient light levels
cartridges combination of various
tests: single cartridge
Amended
Should be single cartridge or
multiple use test cartridges.
However the test parameters
of the cartridges should be
specified in the technical bid.
Additional Point
All test should come simultaneously in a
single test.
Additional point to specification
Amended
All the test parameters
should available in single or
multiple cartridges.
Cartridges for 100 numbers
of blood samples should be
supplied free of cost with the
machine. However, cost of
each type of cartridge for
all parameters for 1000
tests shall have to be
quoted in separate pdf
file which shall be taken
into account of evaluation
and shall be valid during
the warranty period.
ITEM NO.32 (TREADMILL STRESS TESTING)
Page 39 of 49
Review of procurement from the rate
contract
Extra request to procure from
rate contract. Not Accepted
Page No 131 Technical
Specification ECG module:
The analysis frequency should be at
least 8000Hz
Post Test Raw ECG /medians
ECG analysis frequency:500Hz
Re analysis: Post-test medians
measurements from E,J and Post-
J point selection
Amended
ECG analysis
frequency:8000Hz
Re analysis: Post-test
medians measurements from
E, J and Post-J point
selection.
Page No 131 Technical
Specification
ECG Acquisition should be 12 & 16 Lead
& ECG analysis should be available for
12 & 16 analysis
Vector cardiograph (15 lead)
Amended
ECG Acquisition should be 12
& 15/16 Lead & ECG analysis
should be available for 12 &
15/16 analysis.
Page No 131 Technical
Specification Data acquisition:
Sampling rate should be @8000Hz
Sampling rate @4000Hz No Change
The report should be stored in non-
proprietary pdf format and should work
available windows operating system
Complete ECG record and test
results PDF export of final reports
with auto naming protocols also
from Microsoft word and excel
XML export of specified data
network server with editing
workstations \windows XP
operating system
Amended
The ECG record and test
reports should be exported to
PDF format and should be
read in any computer system.
Page No 132 Technical
Specification Display:
Display size should be 22” or more
Monitored leads :3,6,12 &r 15
Displayed Leads: 3,6,12 & 15
Display size :19” or more
Monitored leads :3,6,12 or 15
Displayed Leads: 3,6,12 or 15
No Change
Page No 132 Technical
Specification Display:
Display format: 3rythm ,3rhythm +
medians /raw, 3rhythm + trends,6
rhythm,4 X 2.5 +1 rhythm,2x6
Display format: 3rythm ,3rhythm
+ medians, 3rhythm + trends,6
rhythm,4 X 2.5 +1 rhythm,2x6
No Change
Blood pressure measurement unit and
spo2 unit to be supplied as standard
Vital signs display: Heart rate,
target heart rate ,blood pressure
,exercise clock, stage clock ,phase
clock, protocol ,speed and grade
watts ,METS RRP and spo2
No Change
PrinterLeads:3,6,12 & 15 leads as
standard, NEHB, Cabrera configurable)
PrinterLeads:3,6,12 or 15 leads as
standard, NEHB, Cabrera
configurable)
Amended
PrinterLeads:3,6,12 & 15
leads as standard, NEHB,
Cabrera configurable.
Should be as per manufacturer Height: 148 cm (58 in) with no
monitor installed (LCD display
Amended
Should be as per standard
Page 40 of 49
rotates vertical and horizontal for
optimum viewing
Width :62 cm (24 in) with paper
tray removed
Depth:75cm (30 in)
Weight:68kg without motor
manufacturing design.
Serial ports are old technology and
hence should be removed
Serial ports :6, Com-1-2, COM A-
D, Treadmill, BP, Ergo meter
Spo2
Amended
The serial ports are removed.
ITEM NO.33 (ECG MACHINE)
Page No 134 Technical
Specification
Should have real time display of ECG
wave forms
Should have real time display of
ECG wave forms with signal
quality indication for each lead
Amended
Should have real time display
of ECG wave forms.
Page No 135 Quality standards:
Should be USFDA or European CE
approved product.
Should be USFDA and European
CE approved product. No change
Page No 134 Technical
Specification
Screen size 3” TFT colour HD touch
screen
Should display ECG on LCD/TFT
Display with screen size minimum
5 inch or more.
No change
Page No 135 Technical
Specification Power backup:
up to 8hours at 25mm/h
Additional point to specification
Amendment:
Should have battery back-up
for atleast 2hours at speed of
25mm/hr.
ITEM NO.34 (INFUSION PUMP (VOLUMETRIC))
Page No 135 Product quality
standard
Under product quality standard, the
product should be USFDA or European
CE certified.
Should be USFDA and European
CE approved model.
Amended
Model should be USFDA or
European notified CE
certified.
Page No 135 Technical
Specification Pt. no.1
Screen Size minimum 3inch
monochrome LCD screen/ 4” colour
Or
Large color display. TFT display leads to
specific product
Screen size minimum 4inch TFT
colour HD touch screen
Amended
Screen size should be of 4
inch diagonally colour screen.
Touch screen is not
mandatory.
Page No 135 Technical
Specification Pt. no.2
Operating system: Self-test system
Operating system: System self-
guidance
Amended
The system should have self-
test facility.
Page No 135 Technical
Specification Pt. no.3
Accuracy: ±5%
Or
Accuracy of the pump should be for all
flow rates. Please omit flow rate
Accuracy:>1ml. /hr. ±5%
Amended
Accuracy should of ±5% or
better for all flow rate.
Page 41 of 49
restriction of >1ml/hr.
Page No 135 Technical
Specification Pt. no.4
VTBI /Pre-Set Volume :0 to 9999ml
minimum step is 0.1ml.
Or
0.1-99.99ml increment of 0.01ml.
100.0- 999.0 ml in increment of 0.1ml.
1000-9999ml in increment of 1ml.
VTBI /Pre-Set Volume :0-9999ml
minimum step is 0.01ml
Amended
VTBI /Pre-Set Volume :0 to
9999ml. minimum step is
0.1ml
Page No 135 Technical
Specification Pt. no.5
Total volume infused: 01-9999.99ml
minimum step is 0.1ml
Total volume infused :0.01-
9999.99ml minimum step is
0.01ml
Amended
Total volume infused: 0.1-
9999.99ml minimum step is
0.1ml.
Page No 135 Technical
Specification Pt. no.7
Rate range: 0.1ml/hr to 200ml/hr.
Or
Rate range from 0.1-1200ml/hr.
Rate range 0.01 ml-1200ml/hr
Amended
Should have flow rate range
of 0.1ml./hr. to 1000ml./hr.
or higher.
Page No 135 Technical
Specification Pt. no.10
Infusion mode: 4modes (ml/h: body
weight Micromode, Sequential Mode for
TPN therapy)
Infusion mode:3modes (ml/h:
body weight Micro mode No Change
Page No 135 Technical
Specification Pt. no.11
Infusion rate :20-drops specification
infusion apparatus :0.1 ml/hr to
2000ml/hr. ,60 drops specification
infusion apparatus :0.1 ml.hr to
2000ml/hr.
Infusion rate :20-drops
specification infusion apparatus
:0.01 ml/hr to 1200ml.h ,60 drops
specification infusion apparatus
:0.1 ml.hr to 400ml/hr
Amended
Infusion rate: 60 drops with
flow rate of 0.1 ml/hr to
1000ml/hr.
Page No 135 Technical
Specification Pt. no.16
KVO Rate : Delivery rate >10ml/hr KVO
rate 3ml/h <10ml/hr
KVO rate 1ml/h <1ml/hr
KVO rate default setting 0.1ml/hr.
KVO rate: 0.1 -5.0 ml /h
adjustable default value 1ml/H No Change
Page No 135 Technical
Specification Pt. no.17
Bolus: Auto bolus @ 0.1 -2000ml/hr
with every 0.5ml beep add to the
specification
Bolus: manual and programable
,VTBI 0.1-50ml No Change
Drug Library: Support up to 200
Or
Drug Library: 1500 drugs including all
parameters in drug library upt to 10
users defined drug categories
Drug library: Support 30 drugs
Amended
Should have drug library of
atleast 200 drugs with option
for user defined drug
categories.
History Records: >3000 last history History Records: >5000 last Amended
Page 42 of 49
entries
100 events for system diagnostics.
history entries
History Records: atleast 3000
last history entries
Password protected: supported to be
deleted. Password protected: supported
Amended
Password protected is not
mandatory.
15 kinds of alarm: please elaborate 15 kinds of alarm Amended
Should have alarm facility.
Power supply :9hr at 25ml.hr.: please
elaborate
or
4hours at 100ml/hr with battery
capacity display in h and min
Power supply :9hr at 25ml.h
Amended
Should have battery backup
for atleast 4 hours at flow
rate of 25ml/.hr.
Battery charging Time: ON or \off
status
Battery charging Time: 5hrs
under OFF status
Amended
The point “Battery charging
Time: 5hrs under OFF status”
is deleted.
Other functions: nurse call, RS 232 and
\data export/ Other functions: nurse
call, RS232 and \data export
Other functions: nurse call, RS
232 and \data export & WIFI
SUPPORTED
Amended
The feature of nurse call, RS
232 and \data export & wifi
supported is not mandatory.
ITEM NO.35 (SYRINGE INFUSION PUMP)
Page No 136 Product quality
standard:
The product should be USFDA or
European CE certified.
Should be USFDA and European
CE approved model.
Amended
Should be USFDA or
European notified CE certified
model.
Page No 136 Product quality
standard:
Electrical safety confirms to standards
for electrical safety IEC-60601-1,Class I.
Electrical safety confirms to
standards for electrical safety IEC
60601-1,Class II”
Amended
Electrical safety confirms to
standards for electrical safety
IEC 60601-1 for Class -I and
IEC 60601-2-24.
Pg.136 Technical Specification
(Pt.no.1)
Flow rate Range:0.1 to 200ml/hr
(depending on the syringe capacity –up
to 2000ml/hr,
Or
(up to 1200ml/hr)
or
Flow rate range: 0.01 to 999.9 ml/hr.
Flow rate Range:0.1- 200ml/hr
(depending on the syringe
capacity –up to 1200ml/hr
Amended
Flow rate Range:0.1 to
200ml./hr. with maximum up
to 999.9ml/hr. or more
depending on syringe
capacity.
Pg.136 Technical Specification
(Pt.no.2)
Flow rate accuracy: ≤±2%
Flow rate accuracy: ±1% on
machine, ±2% on syringe
Amended
Flow rate accuracy: ±2% or
better with syringe.
Pg.136 Technical Specification
(Pt.no.3)
Syringe capacity of 5ml. may be added.
Syringe capacities: 10, 20, 30/35,
50/60 CC.
Amended
Syringe capacities: 5ml,
10ml. ,20ml., 30/35ml.,
50/60ml.
Page 43 of 49
Pg.136 Technical Specification
(Pt.no.9)
Auto bolus @ 0.1 -2000ml/hr. with
every 0.5ml beep right next to the
above point of the specification
Or
Delivery rate: 1-1,800ml/hr. max, Bolus
volume 99.99ml Bolus on demand
Bolus with volume /dose
Pre- selection Bolus over time (1min-24
hr.)
Manual bolus Rate 50-1200ml/hr.
(50ml/hr. increment)
Amended
System should have
automatic bolus infusion
facility.
Pg.136 Technical Specification
(Pt.no.10)
Drug library: up to 200 drug name ,add
or delete drugs available in user –
defined drug list.
Or
Drug name display: Drug library with
multiple care area profiles and up to
2000 drug protocol for display during
infusion
Or
1500 drugs can be included.
Drug library: Initial list of 50
agents adjustable with Vigilant
the IV medication Safety
.Adjustment of the dilution
,authorized infusion modes
,default infusion modes flow rate
and limits in ml/hr.
Amended
Should have drug library of at
least 200 drugs or more with
option for user defined drug
categories.
Pg.136 Technical Specification
(Pt.no.11)
Pressure Modes: Dynamic pressure
system with real time pressure with
three or five stage with minimum of 75
mmHg to maximum of 900mmHg.
Or
Pressure setting should be from 50-
1000mmhg in 11 levels of pressure
settings for more precise detection of
occlusion
Or
9 levels from 0.1 bar to 1.2 bar (75
mmHg to 900 mm HG)
Pressure modes: 2 modes
available: variable or 3 pre-set
levels –From 100 to 900 mmHg
,50 mmHg increment
No Change
Pg.136 Technical Specification
(Pt.no.12)
DPS: The Dynamic pressure system
(DPS) warns of pressure variations. A
risk of obstruction or a pressure drop
alarm can be anticipated.
Or
The Dynamic pressure system: DPS –
warns of pressure variations with upper
and lower threshold setting. A risk of
obstruction or a possible leak in the
The Dynamic pressure system
(DPS) warns of pressure
variations. A risk of obstruction or
a possible leak in the infusion line
can thus be anticipated
Amended
The point “DPS: The Dynamic
Pressure System - DPS -
warns of pressure variations.
A risk of obstruction or a
possible leak in the infusion
line can thus be anticipated”
is deleted.
Page 44 of 49
infusion line can thus be anticipated.
Or
Please remove the dynamic pressure
system.
Pg.137 Technical Specification
Pt.14
Battery capacity should be
4hrs/6hr/10hrs. or more instead of
10hrs. at 5ml./hr.
Or
The point may be removed.
Battery capacity minimum: 10
hours at 5 ml/hr.
Amended
Should have battery capacity
of minimum 4 hours at 5
ml/hr.
Pg.137 Technical Specification
Power Supply:
External power 9V DC by a converter is
not required as 5hrs.battery backup of
5hrs.
Power supply:
100 – 240 Vac / 15 VA, external
power 9 Vdc by a converter
Amended
Power supply: 100 to 240
Vac / 15 VA, external power
9V DC by a converter is not
mandatory.
Additional Points:
Ambulance Usage compatibility EN
1789 Water /Dust –proof IP34
Light weight, LCD Display Size 3.0inch
or better visibility.
Volume collection Function: Assist
infused volume record through
automatically volume Calculation with
Four modes:24 Total, Current total,
Time (certain Period)Timing
Volume(Timing interval)
Additional point to specification No Change
The pump should have inbuilt RS 232
port to enable the same to connect to
PDMS/HIS ,if required
Additional point to specification No Change
The pump should have inbuilt drug
dose calculator software and at least 10
levels of occlusion alarm setting
Additional point to specification No Change
Vigilant is proprietary name of a specific
manufacturer. please mention generic
name of software i.e drug error
reduction software and minimum 2000
drug should be configured for better
clinical use
Drug library: Initial drug list of 50
agents adjustable with vigilant
the IV medication safety solution
Adjustment of the dilution
authorized infusion modes,
default infusion modes, flow rate
and bolus limits in ml/hr
Amended
Vigilant/any drug error
reduction software should be
available.
Additional point:
Visibility from 80 degree and
stackability of minimum 3 pumps
Additional point to specification No Change
ITEM NO 36 (PATIENT WARMER)
Pg.137 Technical Specification Pt.2
System should be compatible for
paediatric, infant and adult
Should have Air flow setting for
Adult, Paediatric and infant
patient in same machine
Amended
Should be compatible for
adult, paediatric and infant
Page 45 of 49
patient.
Pg.137 Technical Specification Pt.7
Should have variable Temp. range
from Ambient to 42degree C,±2°Max
Should have variable Temp.
range: Ambient to 42degree
C,±1.5°Max
Amended
Should have variable temp.
range from ambient to
42degree C with ±2°max.
Pg.137 Technical Specification
Pt.10
The blanket should be made of
materials polyethylene film inner layer
and non-woven outer layers or of
similar standard which should be
washable and can be reused
/compatible disposable should be
provided as ours is disposable and
recommended for disposable to avoid
cross contamination
The blanket should be made of
materials polyethylene film inner
layer and non-woven outer layers
or of similar standard which
should be washable and can be
reused.
No change
Pg.137 Technical Specification
Pt.12
The point may be deleted.
Should be compatible during the
use of with blood /Fluid warming No change
Pg.137 Quality Standard
Should be USFDA or CE approved.
Should have safety certificate
from a competent authority CE
(notified) and USFDA (US)
approved.
Amended
Should be USFDA or
European notified CE
approved model.
ITEM NO. 37 (BLOOD/FLUID WARMER)
Pg.138 Quality Standard
Should be USFDA or CE approved.
Should be US FDA and CE
(Notified body) approved model.
Amended
Should be USFDA or
European notified CE
approved model.
Pg.138 Quality Standard
Manufacturer should have ISO9001 or
ISO13485.
Manufacturer should be ISO 9001
& ISO 13485 certified for quality
standards.
Amended
Manufacturer should be ISO
13485 certified for quality
standards.
Pg.138 Quality Standard
The IEC 60601-2-24 should be deleted.
Certified for meting IEC 60601-2-
24: Particular requirements for
the safety of infusion pumps and
controllers.
Amended
Product should meet IEC
60601 standard for general
safety.
Pg.138 Technical Specification Pt.4
Typographical error in temperature.
Temperature should be
maintained at 400C±20C with
accuracy of 10C.
Amended
Temperature should be
maintained at 400C±20C with
accuracy of 10C.
Pg.138 Technical Specification Pt.5
Flow rate of 50-2000ml/hr.
Or
It should be safely and effectively
warms fluids with flow rate minimum
10000ml/hr.
It should be safely and effectively
warms fluids with flow rate of 50
to 2000ml/hr.
No Change
Page 46 of 49
Pg.138 Technical Specification Pt.6
It should be quickly reacts through auto
sensor technology in flow rates
It should be quickly reacts to
changes in flow rate No Change
Pg.138 Technical Specification Pt.7
No disposable set should be asked. Disposable warming set No Change
Should supply a pack of 50 nos. of
consumable tubes /cartridges with the
machine. Cost of 50 nos. of tubes
/plates should be quoted separately in
the financial bid for price evaluation
Should supply a pack of 50 nos.
of consumables tubes/ cartridges
with the machine. Cost of 50 nos.
of tubes /plates should be quoted
separately in the financial bid for
price evaluation.
Amended
Should supply a pack of 50
nos. of consumables tubes/
cartridges/plate with the
machine. Cost of 50 nos. of
tubes /plates/cartridges
should be quoted separately
in the financial bid for price
evaluation.
Single/ dual bag connection facility Dual bag connection facility
Amended
Should have Single or dual
bag connection facility.
Auto/Touch buttons for control Touch buttons for control
Amended
Should have switch or touch
buttons for control.
ITEM NO.39 (PULSE OXYMETER)
Pg.140 Technical Specification Pt.1
LCD display (minimum 3.4”) large
digital display of Spo2.pulse rate and
plethysmogram
LCD display (minimum 4”) large
digital display of SpO2, pulse rate
and plethysmogram
No Change
Pg.140 Technical Specification Pt.5
Compact, portable and easy to set up
with minimum 4Hrs battery backup
Compact, portable and easy to
set up with minimum 4Hrs battery
backup with battery level
indicator
No Change
Pg.141 Quality Standard
USFDA or CE approved
Should have European CE mark
and US FDA approved. No change
ITEM NO.42 (AMBULATORY BLOOD PRESSURE MONITOR)
Measurement method of Asculatory
may be allowed.
Measurement method:
Oscillometric
Amended
Measurement method:
Oscillometric or Asculatory
Equivalent system for data output may
be asked. Data Output RS-232C (Direct)
Amended
Data Output RS 232C
(Direct)/equivalent
USFDA & CE approved USFDA or CE approved Product No Change
Page 47 of 49
Annexure-B
Sl. Queries raised by the prospective bidders
Original Specifications
Clarifications /Amendments of
specification in response to the queries
1 Regarding BG Validity of EMD
Section-III 3.1.3: Bid Details
Note: The EMD may be furnished
in the shape of DD / BG (in shape
of one or multiple DD/BG & the
details of DD (s) / BG (s) are to
be furnished in Format T3). In
case of BG (s), it must be
submitted in the required format
at Annexure V, which is / are to
be valid till 31.01.2019.
Amended
The EMD may be furnished in
the shape of DD / BG (in
shape of one or multiple DD /
BG & the details of DD (s) / BG
(s) are to be furnished in
Format T3). In case of BG (s),
it must be submitted in the
required format at Annexure V,
which is / are to be valid till
Dt. 31.05.2020.
2
120 days from the date of
technically and commercially
clear order, Establishment of
letter of Credit, or site
readiness whichever is later
Section-V Clause 5.1.1 :
Delivery Period
70 days from date of issuance of
Purchase Order
Amended
90 days from date of issuance
of Purchase Order (For Cath
Lab Only)
and
70 days from date of issuance
of Purchase Order (For other
tendered items)
120 days from the date of
opening of commercially clean
letter of Credit
3
For the item Direct Digital
Flat Panel Fluoroscopy &
Radiography System, It
Should have proof of supply of
at least 100% of the tender
requirement (executed directly
by manufacturer /
Importer/authorized
distributor) of the
equipment(s)/ similar
equipment(s) mentioned in the
schedule of requirement to any
Govt. organization / Corporate
Hospitals / PSU Hospitals / UN
Agencies in India/Worldwide
and purchase order copies in
support of that in last 3
Financial years i.e. 2015-16,
2016-17 & 2017-18 (As per
Format T9– Item-wise).
Section-V Clause 5.2
Prequalification of the
Bidders:
(vi) Should have proof of supply
of at least 100% of the tender
requirement (executed directly by
manufacturer /
Importer/authorized distributor)
of the equipment(s)/ similar
equipment(s) mentioned in the
schedule of requirement to any
Govt. organization / Corporate
Hospitals / PSU Hospitals / UN
Agencies in India and purchase
order copies in support of that in
last 3 Financial years i.e. 2015-
16, 2016-17 & 2017-18 (As per
Format T9– Item-wise).
No Change
4
Bid validity of 120 days from
date of opening of technical
bid. As we have to quote in
INR or allow us to quote in US
Section-VI Clause 6.10.1:
Period of validity of bid
The bid must remain valid for
minimum 180 days (six months)
No Change
Clarified
The bid must remain valid for
minimum 180 days (six
Page 48 of 49
dollar from the date of opening of
technical bid for the purpose of
bid evaluation / finalization of
rate contract. As this is rate
contract tender, after finalization
of the rate contract, the approved
rates shall be valid for a period of
one year from the date of
approval of the rate contract. A
bid valid for a shorter period shall
be rejected by the Tender Inviting
Authority as non-responsive.
months) from the date of
opening of technical bid for the
purpose of bid evaluation /
finalization of rate contract
and the bidder have to
quote in INR only.
5
100% confirmed LC out of
which 90% to be paid against
dispatch in the site and 10%
after successful installation and
commissioning of the system
Section-VI Clause 6.30.2 :
Payment:
90% of the cost of the equipment
(excluding CMC Cost) + 100%
installation cost if any + 100%
tax shall be paid to the supplier
on receipt of the stock entry
certificate, installation and
demonstration /training of the
item from the consignee.
Amended
90% of the cost of the
equipment (excluding CMC
Cost) + 100% installation cost
if any + 100% tax shall be
paid to the supplier on receipt
of the stock entry certificate,
installation and demonstration
/training of the item from the
consignee. 90% Payment
can be released through
inland irrevocable Letter of
Credit at sight after
fulfilment of contractual
obligation. (For Cath Lab
only)
100% through irrevocable
Letter of Credit payable 90%
against dispatch document &
10% on installation
Payment should be 100% vide
inland Letter of Credit with
80% payable on delivery &
balance 20% within 30 days of
installation
6
Penalty for Liquidated
Damages should be capped
@5%
Section-VI Clause 6.43.5
Liquidated Damages:
If the successful bidder fails to
deliver any or all of the goods
within the time frame(s)
prescribed in the contract, the
Tender Inviting Authority/User
Institution shall, without prejudice
to other rights and remedies
available to the Tender Inviting
Authority/User Institution under
the contract, deduct from the
contract price / purchase order
price as liquidated damages, a
sum equivalent to 1% of the
value of the item to be supplied
per week of delay or part thereof
on delayed supply of item (s)
until actual delivery or
performance subject to a
No Change
Page 49 of 49
maximum of 4%. Managing
Director, OSMCL reserves the
right to allow an additional penal
period of 4 (four) weeks beyond
the normal penal period (4
weeks) on the written request of
the supplier with the condition
that liquidated damage @ 1.5%
will be charged for each week or
part thereof during the extended
penal period.
N.B:
1. The amendments mentioned above are to be treated as amendments in the general term(s) and
condition(s) and scope of work of the above tender reference. All other terms conditions remain
unchanged.
2. Since any text in the price BOQ can’t be changed in the e-tender portal, the amendments mentioned
above are to be treated as amendments pertaining to price bid/ BOQ (if applicable).
Sd/-
Managing Director
OSMCL
Recommended