Item Schedule No.1 Echo-Cardiography Machine Item Schedule … · 2018-09-11 · Specialty Medical Equipment for Institutions of ESIC, Following corrigendum may please be noted: Item

File No.U-16/30/659/2018-Procell/Super speciality Equipment (704) Dated:11/09/2018

Corrigendum No.2

This is in reference to tender no. U-16/30/659/2012-Procell/Equipment (162) for purchase of Super

Specialty Medical Equipment for Institutions of ESIC, Following corrigendum may please be noted:

Item Schedule No.1 Echo-Cardiography Machine Existing specification Amendment

16.The quoted Model should have CE/FDA Certifications for Quality and also it should have all the certification related to Electrical Safety of the equipment.

The quoted Model should have BIS/European CE/ US FDA Certifications for Quality.

Item Schedule No.2 2D echo Machine with colour Doppler Existing specification Amendment

e.Should be at least CE approved. The quoted Model should have BIS/European CE/ US FDA approved.

Integrated thermal printer. Integrated thermal/ Laser printer.

Item Schedule No.3 Holter with Monitor for analysis Existing specification Amendment

Holter Monitor Holter Monitor

Holter analyzer with following features and software:-

Holter analyzer with following features and software:-

1.Should be a PC based software capable of working with windows 95/98/2000 XP

Should be a PC based software capable of working with windows preferably latest version

4.Hourly count menu, Page scan, mega scan. Hourly count menu, with minimum two scan modes

7.Heart rate variability (HRV) (Time Domian, 3D frequency, Lorenz point care plot.

Heart rate variability (HRV) analysis

10. Possible to have a unique 12 lead analysis with FCG CAD gram.

Deleted

11. Sleep Apnea Monitoring Deleted

14. vectorcardiography Deleted

17. Posssible for electronic enrolment for CF flash card.

Facility for electronic compact technique for Flash card/USB Cable

18. TWA alterns analysis Deleted

Recorders with following configuration:- Recorders with following configuration:-

HQRS. OFFICE

EMPLOYEES’ STATE INSURANCE CORPORATION PANCHDEEP BHAWAN: C.I.G. ROAD: NEW DELHI – 110 002

Tel Fax: 011-23234334, E-mail: [email protected] (An ISO-9001:2008 Certified)

mailto:[email protected]

1. 3-channel digital recorder with removable storage media such CF card-1 no

3-channel digital recorder with removable storage media such CF card/ USB Cable-1 no

3. 7-lead cable-1 no 7 or more lead cable-1 no

System software should consist of:- System software should consist of:-

2.Real time ST analysis in Bar graphs Real time ST analysis

Schedule No.4 Cardiac beds Existing specification Amendment

2. Dimensions of bed Dimensions of bed

Length x width : 2280 mm x 950 mm or better Length : 2200-2290mm approx. and width: 850-1020 mm approx.

Mattress Size : 840 x 2060 mm Appropriate as per bed size

Trendelenburg : 15 degrees or better(electrically) Trendelenburg : 15 degrees approx.

Anti-Trendelenburg : 13 degrees or better(Electrically) Anti-Trendelenburg : 13 degrees approx.

Lateral Tilt : 0-25 degrees or better(Electrically) Lateral Tilt : 0-25 degrees approx.

Height : min. 485 mm or less(electrically) max. 880 mm or better(electrically)

Height : 450-840 mm approx.

Schedule No.6 Hemodialysis machines with all the fluids

Existing specification Amendment

26.Machine should be US FDA approved OR CE certified.

Machine should be BIS/US FDA approved OR CE certified.

Schedule No.12 Electro cautery set with accessories Existing Specifications Amendment

SAME AS UPLOADED SPECIFICATIONS

Unit should comprise of an integerated RF electro surgical unit for electro surgical cut and COAG modes for maximum effects of HF surgery with reusable neutral electrodes with mono polar footswitch with IPX8 certification and reusable bipolar forceps with reusable bipolar cables.

The offered equipments should have brand name /

Model Number embossed / etched on the equipment,

must be supported by Original Literature of the

Original Equipment Manufacturer with mandatory

regional & head office of the Original Equipment

Manufacturer Principal company for providing after

sales service with a dedicated trained service

engineers / service representatives team of O.E.M

Principal company.

The offered equipments accessories & consumables

should be of same offered Original Equipment

Manufacturer.

The electro surgical unit should be microprocessor

controlled, US-FDA & European Certificate marked

in accordance with the medical devices directive

(93/42/EEC), Class I Equipment and

Electromagnetic Compatibility Certificate &

Certificate & ISO Certificate & latest Installation

certificates minimum 50 with satisfactory user list of

minimum 100 installation base in the country.

The electro surgical unit should be micro processor/micro controller based and should adjust the power to get the desired surgical effect on the tissue with facility to use Monopolar under water cutting.

All settings should be controlled by the machine and

according to the tissue deliver.

The electro surgical unit should have power and

voltage automatic regulation feature to prevent

tissue damage and charring.

The output voltage should be regulated in various levels with LCD backlight display for good visibility in operating room , patient plate monitoring facility ,audiovisual alarm and deactivate output if contact between patient and patient plate is not proper to eliminate the risk of patient burn.

It should be programmable and has facility to recall the last setting used by user and should be able to display error

System should have features like Two Monopolar

output socket, One Bipolar Output Socket & Two

Neutral sockets for all types of Reusable &

Disposable Neutral Plates & Voltage and power

regulation in a single system for better coagulation.

System should have following features modes inbuilt -AUTO CUT/ ACE CUT /LOW CUT

-Electrosurgery (ES) cutting with minimal to medium homeostatis . DRY CUT/ BLEND CUT -ES cutting with moderate to intense homeostatis. FORCED COAG/ FULGURATION- effective , fast, pinpoint coagulation . BIPOLAR SOFT COAG/ MICRO/ PRECISE COAG- non sparking , gentle bipolar contact coagulation with minimal sticking and carbonization. SWIFT/ STANDARD COAG - fast aggressive coagulation for dissection with high homeostasis, but limited tissue cutting properties . Uses power dosing/ SPRAY COAG - contact free surface coagulation , low penetration depths.

System should have following features with

Technical Data-

Maximum CUT output - 300 watt at 500 ohm.

Maximum COAG output- up to 200 watt

Frequency- 350 kHz.

System should also have an inbuilt feature with

software for Bipolar Cut & Coagulation facility in

the same unit so that it can be used with

reusable/disposable hand instruments from the OEM

for Open & Laparoscopic Surgeries for faster

Dissection & Coagulation upto 5mm of the vessels.

The electro surgical unit should be supplied with the reusable /disposable Monopolar hand pencil with facility for swapping between programs ( 10 units if reusable or 200 if disposable ) with different set of electrode box (10) no’s, reusable / disposable(20 units) bipolar forceps (bayonet and straight ) with irrigation port and reusable(02 units) / disposable bipolar cable =20 unit each , with monopolar footswitch & having facility for swapping between programs.

Reusable patient plate -Adult and pediatric reusable patient plate cable =02 unit each and if disposable adult and pediatric patient plate 20 box each from the same OEM.

The electro surgical unit should be supplied with the reusable hand instruments and cables from the OEM 2 each / if disposable 50 each of different shapes and length.

Schedule No.13 Uroflowmetery machine with accessories

Existing Specifications Amendment

Must be CE and US FDA approved Must be BIS/European CE/ US FDA approved

Schedule No.14 Upper GI scopes with accessories (Diagnostic) i.e.Monitor, light source, video processor


1B. Should have Chrome endoscopy imaging

(NBI/FICE-BLI/ I scan-OE/m BLU/S technology) and

preferably dual focus Capacity for detailed mucosal

study.

Should have Chrome endoscopy imaging for detailed mucosal study.

1C.Fully immersible in disinfectant solution (resistant cap) and one touch connectivity.

Fully immersible in disinfectant solution with or without (resistant cap) and one touch connectivity.

1I. Depth of field: 4-100 mm or better. Depth of field: 2-100 mm or better.

2a. Reusable biopsy forceps oval cup fenestrated

and oval cup non fenestrated – 2 each

Preferably Reusable biopsy forceps oval cup

fenestrated and oval cup non fenestrated – 2 each

2e.Bipolar Probes-10 Each Bipolar Probes (Optional)-10

2j. Reusable Rotable Clip fixing Device short and

long- 5 each with one hundred single use clip.

Preferably Reusable Rotable Clip fixing Device

short and long- 5 each with one hundred single use

clip.

2k. Extra xenon bulb – 2 Extra xenon/LED bulb – 2 (As per light source)

3A. Should be compatible with analog HD- SDI and

DVI output for HDTV monitor and should contain

electronics for clear visibility of near and far objects.

Should be compatible with analog/digital HD- SDI and DVI output for HDTV monitor and should contain electronics for clear visibility of near and far objects.

3C. Should have Optical chromo endoscopy imaging

such as NBI/FICE-BLI/I scan- OE/mBLU/S

technology and HD plus video

Should have Optical chromo endoscopy imaging

3J. Should have inbuilt light source or separate light source with NBI/FICE-BLI/I scan - OE/m BLU/S technology imaging capacity/ HD plus video.

Should have inbuilt light source or separate light source.

3K. High intensity Xenon light source (300W) with

500 hours life with emergency halogen light for backup High intensity Xenon light source (300W) minimum 500 hours life/LED light source with emergency light for backup

3M. Should be supplied with two extra xenon bulbs

and one extra halogen bulbs Deleted

3O.Video signal output : RGB, Y/C and composite

(Simultaneous) Should have Video signal output

3P. Should be supplied with 2kw online UPS Should be supplied with minimum 2kw online UPS

3Q. Video endoscopy workstation with space for

accommodation of a LCD video monitor (26” or more

in size), video processor, light source with scope

hanger

Video endoscopy workstation with space for

accommodation of a video monitor (24” or more in size),

video processor, light source with scope hanger

4. High definition Medical Grade LED monitor(From the same parent manufacturer of the scope)

High definition Medical Grade monitor (Compatible with the scope)

4A.26 inch full HD LED monitor with high resolution 1920× 1080

24 inch or more full HD monitor with high resolution

The complete system should be European CE or US FDA approved, other than the suction machine

The complete system should be BIS/European CE or US FDA approved, other than the suction machine

Schedule No.15 Upper GI scopes with accessories (Theraputic) i.e. Monitor, light source,

video processor


1B. Should have Chrome endoscopy imaging

(NBI/FICE-BLI/ I scan-OE/m BLU/S technology)

and preferably dual focus Capacity for detailed

mucosal study.


1K. Instrument channel: > 3.8 mm Instrument channel: > 3.2 mm





2e. Bipolar Probes-10 Each Bipolar Probes (Optional)-10

2j. Reusable Rotable Clip fixing Device short and

long- 5 each with one hundred single use clip.

Preferably Reusable Rotable Clip fixing Device

short and long- 5 each with one hundred single use

clip.

2k. Extra xenon bulb – 2 Extra xenon/LED bulb – 2

3HH. Video signal output : RGB, Y/C and

composite (Simultaneous)

Should have Video signal output

4E. 26 inch full HD LED monitor with high resolution 1920× 1080

24 inch or more full HD LED monitor with high resolution 1920× 1080

2b. Hot Biopsy forceps with alligator cups with and without needle- 3each

Hot Biopsy forceps with alligator cups with and without needle- 2 each

2e. Bipolar Probes-10 Each Bipolar Probes (Optional)-10

2g. Washing pipe/ spray catheter – 20 Washing pipe/ spray catheter – 10

2k. Extra xenon bulb – 2 Extra xenon/LED bulb – 2

3T. Should be compatible with analog HD- SDI and DVI output for HDTV monitor and should contain electronics for clear visibility of near and far objects.


3V. Should have Optical chromo endoscopy imaging such as NBI/FICE-BLI/I scan- OE/mBLU/S technology and HD plus video.


3CC. Should have inbuilt light source or separate light source with NBI/FICE-BLI/I scan - OE/m BLU/S technology imaging capacity/ HD plus video.

Should have inbuilt light source or separate light source

3DD. High intensity Xenon light source (300W) with 500 hours life with emergency halogen light for backup

High intensity Xenon light source (300W) with minimum 500 hours life/LED light source with emergency light for backup

3FF. Should be supplied with two extra xenon bulbs and one extra halogen bulbs

Deleted

3HH. Video signal output : RGB, Y/C and composite (Simultaneous)

Should have Video signal output

3JJ. Video endoscopy workstation with space for accommodation of a LCD video monitor (26” or more in size), video processor, light source with scope hanger

Video endoscopy workstation with space for accommodation of a video monitor (24” or more in size), video processor, light source with scope hanger


High definition Medical Grade monitor (compatible with the scope)

4E. 26 inch full HD LED monitor with high resolution 1920× 1080

24 inch or more full HD monitor with high resolution 1920× 1080



Schedule No.16 Electro cautery machine Existing Specifications Amended Specifications


Unit should comprise of an integerated RF electro surgical unit for electro surgical cut and COAG modes for maximum effects of HF surgery with reusable neutral electrodes with mono polar footswitch with IPX8 certification and reusable bipolar forceps with reusable bipolar cables.

The offered equipments should have brand name /

Model Number embossed / etched on the equipment,

must be supported by Original Literature of the

Original Equipment Manufacturer with mandatory

regional & head office of the Original Equipment

Manufacturer Principal company for providing after

sales service with a dedicated trained service

engineers / service representatives team of O.E.M

Principal company.

The offered equipments accessories & consumables

should be of same offered Original Equipment

Manufacturer.

The electro surgical unit should be microprocessor

controlled, US-FDA & European Certificate marked

in accordance with the medical devices directive

(93/42/EEC), Class I Equipment and

Electromagnetic Compatibility Certificate &

Certificate & ISO Certificate & latest Installation

certificates minimum 50 with satisfactory user list of

minimum 100 installation base in the country.

The electro surgical unit should be micro processor/micro controller based and should adjust the power to get the desired surgical effect on the tissue with facility to use Monopolar under water cutting.

All settings should be controlled by the machine and

according to the tissue deliver.

The electro surgical unit should have power and

voltage automatic regulation feature to prevent

tissue damage and charring.

The output voltage should be regulated in various levels with LCD backlight display for good visibility in operating room , patient plate monitoring facility ,audiovisual alarm and deactivate output if contact between patient and patient plate is not proper to eliminate the risk of patient burn.

It should be programmable and has facility to recall the last setting used by user and should be able to display error

System should have features like Two Monopolar

output socket, One Bipolar Output Socket & Two

Neutral sockets for all types of Reusable &

Disposable Neutral Plates & Voltage and power

regulation in a single system for better coagulation.

System should have following features modes inbuilt -AUTO CUT/ ACE CUT /LOW CUT

-Electrosurgery (ES) cutting with minimal to medium homeostatis . DRY CUT/ BLEND CUT -ES cutting with moderate to intense homeostatis. FORCED COAG/ FULGURATION- effective , fast, pinpoint coagulation . BIPOLAR SOFT COAG/ MICRO/ PRECISE COAG- non sparking , gentle bipolar contact coagulation with minimal sticking and carbonization. SWIFT/ STANDARD COAG - fast aggressive coagulation for dissection with high homeostasis, but limited tissue cutting properties . Uses power dosing/ SPRAY COAG - contact free surface coagulation , low penetration depths.

System should have following features with

Technical Data-

Maximum CUT output - 300 watt at 500 ohm.

Maximum COAG output- up to 200 watt

Frequency- 350 kHz.

System should also have an inbuilt feature with

software for Bipolar Cut & Coagulation facility in

the same unit so that it can be used with

reusable/disposable hand instruments from the OEM

for Open & Laparoscopic Surgeries for faster

Dissection & Coagulation upto 5mm of the vessels.

The electro surgical unit should be supplied with the reusable /disposable Monopolar hand pencil with facility for swapping between programs ( 10 units if reusable or 200 if disposable ) with different set of electrode box (10) no’s, reusable / disposable(20 units) bipolar forceps (bayonet and straight ) with irrigation port and reusable(02 units) / disposable bipolar cable =20 unit each , with monopolar footswitch & having facility for swapping between programs.

Reusable patient plate -Adult and pediatric reusable patient plate cable =02 unit each and if disposable adult and pediatric patient plate 20 box each from the same OEM.

The electro surgical unit should be supplied with the reusable hand instruments and cables from the OEM 2 each / if disposable 50 each of different shapes and length.

Schedule No.17 Low GI (colonoscope) Existing Specifications Amendment

1O. Should have Chrome endoscopy imaging (NBI/FICE-BLI/ I scan-OE/m BLU/S technology) and preferably dual focus Capacity for detailed mucosal study.


1P. Fully immersible in disinfectant solution (resistant cap) and one touch connectivity.


1V.Depth of field: 4-100 mm or better. Depth of field: 2-100 mm or better.

1X. Instrument channel: 3.8 mm (approx) Instrument channel: 3.7 mm or more





2c. Polypectomy snare hexagonal and oval rotatable (2 Pack of 10 each)

Polypectomy snare hexagonal/oval rotatable (2 Pack of 10 each)

2e. Multibite biopsy forceps- 5 Nos Multibite biopsy forceps(Optional)- 5 Nos

2k. Extra xenon bulb – 2 Extra xenon/LED bulb – 2 (According to light source)

3MM. Should be compatible with analog HD- SDI

and DVI output for HDTV monitor and should

contain electronics for clear visibility of near and

far objects.


3OO. Should have Optical chromo endoscopy

imaging such as NBI/FICE-BLI/I scan-

OE/mBLU/S technology and HD plus video and

HD plus video.


3VV. Should have inbuilt light source or separate

light source with NBI/FICE-BLI/I scan - OE/m

BLU/S technology imaging capacity/ HD plus

video.

Should have inbuilt light source or separate light source

3WW. High intensity Xenon light source (300W)

with 500 hours life with emergency halogen light

for backup

High intensity Xenon light source (300W) with minimum 500 hours life/LED light source with emergency light for backup

3YY. Should be supplied with two extra xenon

bulbs and one extra halogen bulbs

Deleted

3AAA. Video signal output : RGB, Y/C and

composite (Simultaneous)

Should have Video signal output facility

3BBB. Should be supplied with 2kw online UPS Should be supplied with minimum 2kw online UPS

3CCC.Video endoscopy workstation with space for accommodation of a LCD video monitor (26” or more in size), video processor, light source with scope hanger.

3CCC.Video endoscopy workstation with space for accommodation of a video monitor (24” or more in size), video processor, light source with scope hanger.


High definition Medical Grade monitor (compatible with the scope)

4I. 26 inch full HD LED monitor with high resolution 1920× 1080

24 inch or more full HD monitor with high resolution



Schedule No.18 Sigmoidoscope Existing Specifications Amendment

Fully immersible in disinfectant solution (resistant cap) and one touch connectivity.


1D. Depth of field: Near 2-3mm or better and Far 4-100 mm or better.

Depth of field:2-100 mm or better.

1F. Instrument channel: > 3.8 mm (approx) Instrument channel: > 3.7 mm (approx)

1G. Working length: 790 mm (approx) Working length: 630 mm or more

1H. Total length: 1090 mm (approx) Total length: 1090 mm or more

2a. Reusable biopsy forceps oval cup fenestrated and oval cup non fenestrated – 2 each

Preferably Reusable biopsy forceps oval cup fenestrated and oval cup non fenestrated – 2 each

2f. Extra xenon bulb – 1 Extra xenon/LED bulb – 1 (According to light source)

Schedule No.20 APC (argon plasma coagulator) Existing Specifications Amendment

1.2 Modes of operation: Foot switch and handswitch Modes of operation: Foot switch

2.1 Provision for connection of two cylinders of gas of 2 – 5 L

Provision for connection of preferably two cylinders of 2 – 5 L

2.6 Option of flushing with flushing duration of 5 seconds or less

Deleted

3.1 APC probe should be reusable, sterilizable and washable

APC probe should be preferably reusable, sterilizable and washable

3.4 Different catheters : Length 1.5 meters to 2.5 meters ( Straight beam) – 2 Length 1.5 meters to 2.5 meters ( Side conical) – 2

Different catheters : Length 1.5 meters to 2.5 meters ( Straight beam), Length 1.5 meters to 2.5 meters ( Side conical)- 2 each

Schedule No.21 EEG with brain mapping machine Existing Specifications Amendment

2.1. Should be a 32 Channel digital EEG Machine,

where 24 Channels for acquisition and storage, 5

Polygraph and 3DC Channels.

Should be a 32 Channel digital EEG Machine, where 24

Channels for acquisition and storage, 5 Polygraph and 2

or more DC Channels.

2.2. Frequency response should be 0.05 HZ to 70 HZ. Frequency response should be 0.05 HZ to 500 HZ.

2.10. Should have HLF (15.35 .70 Hz) and LLF (0.1,0.3,1.5,3.5 Hz) filters for each channel as well as for all channel for display.

Should have HLF (05-500 Hz) and LLF (0.05-5 Hz) filters for each channel as well as for all channel for display.

37. Should have safety certificate from a competent

authority CE FDA (CS) STQC, CB certificate. STQC S

certificate of valid detailed electrical and functional

safety test report from ERTL. Copy of the certificate

test report shall be produced along with the technical

bid.

Should have safety certificate from BIS/European CE/US

FDA

Schedule No. 22 NCV machine & EMG with evoked potential


2.1. Minimum 4 channel system with optical isolation with Ethernet connection for connecting to either to desktop system or laptop system for portable use.

Minimum 4 channel system with optical isolation with Ethernet/USB connection for connecting to either to desktop system or laptop system for portable use.

4.1. Should be FDA, CE, UL or BIS approved product. Should be BIS/US FDA/European CE approved .

Schedule No.23 Bed side Multipara Monitor Existing Specifications Amended Specifications

SAME AS UPLOADED SPECIFICATIONS should be modular monitor with more than 12 inch TFT display with 8 or more waveforms monitoring facility

Should have compact design of module to measure parameters like ECG, NIBP,HR, Resp, SPO2, 2X TEMP, Main stream/Side stream ETCO2(low flow/micro stream), 2X IBP for monitoring adult , paediatric and neonate patients

Monitor should have inbuilt or rechargeable batteries for minimum two hours.

Should have standard technology for SPO2 measurement - MASIMO/NELCOR. Should be able to measure SPO2 in low perfusion/with motion artifacts.

Monitor should have Arrhythmia detection, S-T analysis and pacemaker detection

Should be upgradable to and company should quote for following modules: anaesthesia multi gas (main stream), CO, BIS & NMT along with cost of accessories

min 72 hrs graphical and tabular trends of all parameters

Confirms USFDA/European CE/BIS certification for quality standards (Quoting Company should furnish USFDA certificate specific to model quoted / CE /BIS certification)

Should be supplied with 3/5 lead ECG cable for arrhythmia and ST analysis and pacemaker detection , NIBP cuff adult, paediatric & child Two no each , SPO2 sensor adult, paediatric & neonatal 5 no each, skin & nasopharyngeal temperature sensor 1 no. each, 10 ETCO2 sample lines, 2 No’s of Reusable IBP interface cables and 20No’s of Disposable IBP transducers, suitable wall mount

ECG

Leads 3 to 5 provision for 12 lead ECG along with print out facility protection from the interface of electrosurgical apparatus, wave form ECG or SPO2 selectable ,arrhythmia detection , heart rate detection from ECG/pulse auto change

Spo2 range from 0% to 100% ( accuracy +/- 2%). Sensitivity should be good waveform ECG or SPO2 selectable / auto/auto-change should be supplied with proper probes( 10 each)for neonatal paediatric and adult patients

NIBP range: neonate / paediatric to adult, modes auto/ manual numeric display: systolic diastolic, mean. Should be supplied with proper size 5 cuffs each for neonatal, pediartic,adult and extra-large for obese patients

Provision of two simultaneous measurement of IBP. Display waveform and numeric 50 universal transducer sets to be supplied

TEMPERATURE

Dual temperature monitoring( core and skin)with sensor cable and probes

ETCO2

Infra-red side stream analyser for CO2, capable of monitoring ETCO2 of intubated patient, display : waveform and digital. range : 0 to 15 vol% or 0 to 15 kpa or 0 to 113 mmhg

ALARMS

Asystole, arrhythmia,leads off,SPO2 probe disconnection , BP cuff occlusion, apnoea, ETCO2 alarms

Schedule No.24 Arterial Blood Gas Analyser Existing Specifications Amended Specifications

SAME AS UPLOADED SPECIFICATIONS 1. The Instrument should be fully automated blood

gas along with electrolyte analyzer.

2. Instrument should be able to measure accurately within clinical range and resolution of the following measured parameters pH, pCO2, pO2, Sat O2 (SO2), tHb / Hct, Na+, K+, Ca++, Cl, Barometric pressure.

3.It should also have following calculated

parameters:

a. PH /Pco2 /pO2 corrected to patients

temperature.

b. Hematocrit

c. HCO3

d. Standard HCO3,

e. Base Excess of blood(BE)

f. Calculated Parameters SaO2,Bicarb

(HCO3),Std.HCO3,Base excess of blood (BE),Base excess of Extracellular fluid (BE-ECF),Hct (calculated from +Hb),Base Buffer (BB) etc.

g. Oxygen content (O2 Ct)

h. Total O2 content(T CO2)

i. O2 carrying capacity

j. Functional O2 Saturation calculated with P50 as

default value (P50 / SO2(c)

k. Anion gap

l. Hematocrit calculated from Total Hb{Hct(c)}

m. P/F index PaO2/FIO2 ratio

4

a. Instrument should be fully automatic with

technology for accurate measurement.

b. Automatic 1 point, 2 point (of all measured

parameters) and system calibration by liquid

calibrators (without use of any gas cylinders,

Humidifiers and cassettes) with programmable

calibration frequencies.

c. Automatic rinsing after every measurement

/calibration.

d. Automatic cleaning and system alignment at

regular intervals.

e. Instrument should have a standby mode

(economy mode) with auto wake up facility to

optimise the reagent utilization.

f. The instrument should have facilities like monitor

screen/minimum 17" wide touch screen keyboard/numeric keypad and barcode reader.

g. All results should be microprocessor controlled

and of latest technology version.

h. Maintenance free electrodes with individual electrodes

on/off facility and Built in auto QC facility

5. Fully automatic liquid calibration of all parameters at user defined intervals without the use of gas calibrated reagents , External gases, Tanks or regulator.

6. Sample: All parameters should be measured in

single injection /aspiration of sample directly from

syringe or capillaries. The instrument should accept

heparinised arterial, mixed venous and capillary

whole blood. It should also provide the facility to

measure the above measured and calculated

parameters in gases, cerebrospinal fluid, dialysate

and pleural fluid, QC material etc.

7. should have input parameters a) Patient –ID, name …..Age, Sex, Sample Type-

8.Result: All results should be accurate and to be available in about 1-3mins.Data display on well illuminated ,adequate size LCD color touch screen display. Data printout on built -in graphic printer/capable of attachment to external printer through RS 232 port. Analyzer with memory of storing patient data/result minimum 250 or more

9. Instrument to be provided with

a) Protective acrylic cabinet with standard

accessories.

b) Compatible Online UPS with battery backup of

at least 2 hour.

c) Start-up kits

d) Calibrators

e) Electrodes

f) QC materials 3 level each.

g) Capillaries suitable for paediatric samples for 500

patients.

h) All other required consumables including thermal paper sufficient for six months according to 25 samples

10. Essential components:

a. Electrodes: Maintenance free electrodes with separate on/off facility. The electrodes should be replaced free of cost during warranty period and the prices should be frozen for next five years.

b. Reagents: Continuous reagent level monitoring with

graphic display and onboard life of reagents should not be one month

11. Software:

a. Display language should have English mode.

b. Compatible software to communicate data

between ABG machine and host computer.

c. It should have advanced software video

tutorials, multitasking to lower down time, interface

with internet and computer network auto restart after

maintenance, online help two way communication

possibility to unite operatorsnte. The instrument

should have capability to interface a computer and

data acquisition and patient record with software in

use /recommended. The system should have RS 232

serial port.

d. Reference and critical ranges should be

configured based on age, sex, sample type etc.

e. Data storage of minimum 250 patients/QC results or

more.

12. All support for integration with existing data on

host computer in must

13. Waste bag: the waste container should be sealed

to prevent operator biohazard

14. Backup power supply: UPS system for blood gas

analyzer for a minimum of 2 hours back up.

15. Power required: 110-240v, 50-60 HZ. There

should be storage facility of data in case of power

failure.

16. It should follow the international safety and ISO

standard requirements.

17. Enclosed users list with date of installation,

address and contact numbers.

18. All standard accessories should be provided

19. Demonstration is compulsory

20. Training to staff at site-should be provided.

21. Operating and detailed service manual should be

provided.

22.Operating room temperature between 15-35

degrees Celsius and so for maintaining the optimum

temperature and for smooth running of the machine

one SPLIT AC 2Ton Capacity must be supplied free

along with the machine .

23. All the required reagents for investigation on ABG with electrolyte analyzers should be provided free of cost @10 samples per day for 6months or 1800 samples, whichever is earlier. The price for the reagent should be freezed for further 5 years after the warranty of 5 years.

24. Should have local service facility ( within about 50 km radius from the place of installation) and should have the necessary equipments recommended by the manufacturer to carry out maintenance as per guidelines provided in maintenance manual.

25. PM Kit:PM Kit containing all the consumables

like tubing, electrodes, light source, needles, fill

port, peristaltic pump should be supplied free

regularly for 2 years. Cost of electrodes /sensors,

tubing and spares should be quoted separately.

26.WARRANTY: warranty of 5 years including of all spares, electrodes, sensors, pump tubing, full port, needles etc. Expected on board life of all electrodes /sensors, tubing and spares should be quoted separately.

28. Should have certificate from a Competent Authority-European CE/US FDA/ST QC certificate or valid detailed electrical and functional safety report from ERTL. Copy of certificate/test report shall be produced along with technical bid.

29. Bidder should specify per test cost in technical bid.

Schedule No.25 Transport / Portable (Ventilator) Existing Specifications Amended Specifications

SAME AS UPLOADED SPECIFICATIONS Specifications

Technical characteristics

Modes of ventilation: a) Volume controlled, b) pressure controlled, c) pressure support,

d) synchronized intermittent mandatory ventilation (SIMV),

e) Assist/ control mode,

F) PEEP

Alarms required: FiO2, minute volume, pressure, PEEP, apnoea, occlusion, high respiration rate, disconnection

System alarms required: Power failure, gas disconnection, low battery, vent inoperative, self diagnostics

If alarm silencing feature is incorporated, it must be temporary and clearly display when activated

Air and externally supplied oxygen mixture ratios fully controllable

Inlet gas supply (O2) pressure range at least 35 to 65 psi

Medical air compressor integral to unit, with inlet filter

Visual and audible alarms. Accessories and tubing should be supplied for adult, paediatric & neo-natal size requirement

Settings: The following variables should be controlled by the operator

a) tidal volume up to 50ml-1400ml / more

b) Pressure (inspiratory) up to 50cm H2O

c )Volume (inspiratory) up to 120 l/min

(d) Respiratory rate: up to 60 breaths per minute

(e) SIMV respiratory rate: up to 40 breaths per minute (f) PEEP up to 20 cm H20,

(g) Pressure support up to 45 cm H2O,

(h) FiO2 between 21 to 100%, (i) Inspiratory and expiratory times up to at least 2 sec and 8 sec respectively

Users interface: Manual and automatic

Inbuilt software and/or standard of communication (where ever required)

Physical characteristics

Weight should be less than 5 kg

Alarm more than 65 dB

Should be portable

Energy source

Power requirement: 220 to 240 V, 50 Hz

Battery operated with at least 6 hours of battery backup

Tolerance (to variation, shutdowns): plus or minus 10% input AC

Electrical protection by resettable over current breakers or replaceable fuses, fitted in both live and neutral lines

Protection: OVP, earth leakage protection and Electrical protection by SMPS

Power consumption should not be more than 140 w

Other energy supplies: Gas/battery driven

Accessories and spare parts, consumables ,Full face mask, breathing circuit for adult, paediatric sizes, carry bag, filters Battery, leakage adaptor tubing should be supplied

Environmental and Departmental considerations

Cleanable with alcohol or chlorine wipes

Standards and safety

European CE /US FDA/BIS certified

Training and installation

Pre-installation requirements: Electrical sockets, oxygen supply

Supplier to perform installation, safety and operation checks before handover. Local clinical staff to affirm completion of installation

Training of users in operation and basic maintenance shall be provided. Advanced maintenance tasks required shall be documented

Warranty and maintenance

5 years warranty

Maintenance manual detailing complete maintaining schedule

Warranty of five years with free servicing (Min 3) during warranty

The spare price list of all spares and accessories (including minor) required for maintenance and repairs in future after guarantee/ warranty period should be attached

Documentation

User, technical and maintenance manuals to be supplied in English language

Certificate of calibration and inspection to be provided

List to be provided of equipment and procedures required for local calibration and routine maintenance

List to be provided of important spares and accessories, with their part numbers and cost.

Any warning signs would be adequately displayed

Service centre details

Contact details of manufacturer, supplier and local service agent to be provided

Ventilator should run on air compressor /Turbine technology

Schedule No.26 Invasive Mechanical Ventilator Existing Specifications Amended Specifications

4a. Tidal Volume: Minimum 5 ml and maximum at least 1500 ml or more in Volume control.

Tidal Volume: Minimum 2 ml and maximum at least 1500 ml or more in Volume control.

13. Event log: 1000 Alarm History Event log: up to 1000 Alarm History

14. Demonstration is must Deleted

15. Spares should be available for 10 years. Deleted

17. LIS-FDA, CE approved. European CE /US FDA/BIS certified

18. Ventilator should have external compressor, from the same manufacturer.

Ventilator preferably should have external compressor, (from the same manufacturer).

21.Compressor should be US-FDA approved. European CE /US FDA/BIS certified

Schedule No.27 Non-Invasive Mechanical Ventilator/Bi PAP and CPAP

Existing Specifications Amended Specifications

17.Machine should be fitted with electrostatic fibre mesh air filter.

Deleted

22.Should have safety certificate from a competent authority CE issued by a notified body registered in European commission / FDA (US)

Should have safety certificate from European CE /US FDA/BIS certified

Schedule No.28 Defibrillator/with monitor/with recorder with external pacemaker



1. The machine should have the facility for ECG monitoring, defibrillation, external pacing (transcutaneous) and recorder.

2. The defibrillator should be biphasic technology, having energy selection upto maximum 200 joules in AED as well as in manual mode

3. It must be capable of monitoring ECG through ECG cables ,multi function electrodes and paddles through multifunction single cable

4. The machine should be able to defibrillate adult ,pediatric patients.

5. The machine should have ECG waveform display on bright high resolution display.

6. The machine should be compact, portable within built rechargeable battery. The machine should not be more than 7 Kgs with battery and paddles.

7 The machine should have in built recorder printing ECG trace & stored information.

8 The machine should have a facility of External non-invasive pacing with 40ms pulse width

9 It should have ability to measure chest compression rate and depth in real time with visual feedback on screen with rate and depth indicator.

10. The machine should have user selectable alarm settings.

11. The machine should work on mains as well as on rechargeable battery.

12. The unit should be supplied with Adult and in built paediatric external paddles. The machine should have facility to increase or decrease energy selection on unit and charge or discharge facility on paddles as well as unit. The unit should also have facility to give printout of ECG and shock instantly from paddles.

13. Charging time should be less than 6 to 7 sec at maximum energy.

14. The unit should be supplied with following accessories/item

a)Battery-1nos b)3-Lead ECG cable -1nos

c) External defibrillator paddles (paediatric in built in adult)-1nos

d)Multi Function Defibrillator & Monitoring pads/gelsheets-200nos

e) Reusable CPR feedback sensor/or similar product reused at least on 90 patients.

15. The unit should be upgradeable to monitor EtCO2, NIBP & SPO2

16. Also the unit should be upgradable to12 lead ECG monitoring if required.

17. The unit should be USFDA/European CE/BIS certified.

Schedule No.29 Intermittent Pneumatic Compression Device


2. It should be US FDA OR CE (Conformite European) approved.

It should be BIS/US FDA/ European CE approved.

Existing Terms & Conditions Amended Terms & Conditions Performance security/unit:Fixed as per Schedule no. of item

Performance security/unit: 10% of actual cost of equipment

5.2 The validity of the Bank Guarantee will be for a period up to sixty (60) days beyond Warranty Period.

The validity of the Bank Guarantee will be for a period up to sixty (60) days beyond CMC Period.

5.3 In the event of any failure /default of the supplier with or without any quantifiable loss to the government including furnishing of consignee wise Bank Guarantee for CMC security as per Proforma in Section XV, the amount of the performance security is liable to be forfeited.

In the event of any failure /default of the supplier with or without any quantifiable loss to the ESIC including furnishing of consignee wise Bank Guarantee for CMC security as per Proforma in Section XV, the amount of the performance security is liable to be forfeited.

5.6 Subject to GCC sub – clause 5.3 above, the Purchaser/Consignee will release the Performance Security without any interest to the supplier on completion of the supplier‘s all contractual obligations including the warranty obligations & after receipt of Consignee wise bank guarantee for CMC security in favour of Head of the Hospital/ Institute/ Medical College of the consignee as per the format in Section XV.

Subject to GCC sub – clause 5.3 above, the Purchaser/Consignee will release the Performance Security without any interest to the supplier on completion of the supplier‘s all contractual obligations including the CMC obligations

15.The warranty shall remain valid for a period of 5 years as mentioned the date of installation & commissioning with a regular updates of newer technology as and when evolved followed by a CMC for a period of 5 (Five) Years for all the equipment after the goods or any portion thereof as the case may be, have been delivered to the final destination and installed and commissioned at the final destination and accepted by the purchaser/ consignee in terms of the contract, unless specified otherwise in the SCC.

The warranty shall remain valid for a period of 5 years as mentioned the date of installation & commissioning with a regular updates of newer technology as and when evolved followed by a CMC for a period of 5 (Five) Years for all the equipment after the goods or any portion thereof as the case may be, have been delivered to the final destination and installed and commissioned at the final destination and accepted by the purchaser/ consignee in terms of the contract, whereever specified in the SCC/Item schedule or anywhere in tender enquiry.

SECTION – XV BANK GUARANTEE FORM FOR PERFORMANCE SECURITY/ CMC SECURITY This guarantee shall be valid till such time to cover two months beyond the warranty period from the date of Notification of Award i.e. up to _____________ (indicate date).

SECTION – XV BANK GUARANTEE FORM FOR PERFORMANCE SECURITY/ CMC SECURITY This guarantee shall be valid till such time to cover two months beyond the CMC period from the date of Notification of Award i.e. up to _____________ (indicate date).

SECTION – XVI CONTRACT FORM - A CONTRACT FORM FOR SUPPLY, INSTALLATION, COMMISSIONING, HANDING OVER, TRIAL RUN, TRAINING OF OPERATORS & WARRANTY OF GOODS

SECTION – XVI CONTRACT FORM - A CONTRACT FORM FOR SUPPLY, INSTALLATION, COMMISSIONING, HANDING OVER, TRIAL RUN, TRAINING OF OPERATORS & WARRANTY OF GOODS In case of Authorised dealer participate in the bidding process SECTION – XVI CONTRACT FORM - should also be countersigned by OEM/Manufacturer

CONTRACT FORM – B CONTRACT FORM FOR ANNUAL COMPREHENSIVE MAINTENANCE CONTRACT

CONTRACT FORM – B CONTRACT FORM FOR ANNUAL COMPREHENSIVE MAINTENANCE CONTRACT In case of Authorised dealer participate in the bidding process SECTION – XVI CONTRACT FORM - B should also be countersigned by OEM/Manufacturer

Add: All the equipments (Schedule No.1 to schedule No.29) should be BIS/European CE/US FDA certified

TEC can take decision regarding selection/non selection of the quoted items after verification/ evaluation and working demonstration of the quoted equipment(s).

Bank detail and account no. Branch code-9017 Syndicate Bank Account No.90172010131946 IFSC Code-SYNB0009017 MICR CODE-110025021

This issues with the approval of Competent Authority.

DMC (PC & RC Cell)

Documents

Item Schedule No.1 Echo-Cardiography Machine Item Schedule … · 2018-09-11 · Specialty Medical Equipment for Institutions of ESIC, Following corrigendum may please be noted: Item