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Revo
xSte
riliz
atio
n.co
m©
2015
MAR
CORA
ll Righ
ts Re
serve
d. PN
XXXX
X-XXX
/ARE
VOX®
is a
regist
ered t
radem
ark of
MAR
COR,
ACan
tel M
edica
l Com
pany
.
REVO
X St
erili
zati
on S
olut
ions
1460
5 28
th A
venu
e N
orth
Min
neap
olis
, MN
554
47
Make it possible.
Just-In-Time Sterilization.™
It’s about time.
REVOX 417L
Gentle room-temperature process
No harmful residuals—VPA chemistry breaks down into CO2, H2O, and O2
No lengthy pre-conditioning or post-processing aeration required
Compatible with a broad range of materials and packaging
Fast turnaround contract sterilization services
�Expert�guidance�to�meet�technical,�operational,�and�financial�project objectives
Technical support and on-site maintenance provided by a nationwide service network
The REVOX™ 417L uses a room-temperature vaporized peracetic acid (VPA) sterilant, injected into a variable vacuum sterilization chamber under controlled conditions. REVOX Sterilization Solutions’ unique�processes�and�flexible�operational�capabilities�allow�for�the�routine�execution�of�traditionally�difficult�sterilization�cycles.
Introducing the REVOX™ 417L. Gain the advantage of on-site sterilization�with�a�room-temperature,�cost-effective,�and�efficient�sterilization�solution.�You’ll�save�time,�money,�and�critical logistical capacity.
Put a time machine in your production line.
It’s about time your sterilization process matches your potential.For decades, sterilization has been one of the most inefficient steps in the medical manufacturing process, limiting your full competitive potential. Outsourcing the process to off-site contractors has typically meant dealing with significant logistical challenges, long lead times, and bottlenecks in the production process which can wreak havoc with modern-day continuous improvement objectives. And attempting to handle sterilization on-site has required installing enormously expensive and potentially hazardous sterilization processes—like gamma irradiation or ethylene oxide (ETO)—in your facility. But imagine a safer, more affordable sterilization process housed under your own roof, one that’s compatible with today’s wider array of medical materials and also fully capable of meeting your just-in-time manufacturing needs.
Introducing the REVOX™ 3000L, a game-changing solution that
represents the first leap forward in the scalability of efficient, on-site just-in-time sterilization.™ Thanks to its patented room temperature vaporized Peracetic Acid sterilization
process, REVOX sterilization offers class-leading materials compatibility and packaging flexibility. And with its new, seven-fold larger capacity and 2-4 hour cycle times the 3000L also accommodates highproduction throughput and quickerturn-arounds. In other words, the REVOX 3000L sterilization solution truly represents the best of both worlds for medical manufacturers—allowing you to finally achieve your full potential for optimal operational efficiency and product innovation.
Technical Specifications
Usable Volume 96 cubic ft.
Physical Dimensions 302 cm x 218 cm x 213 cm (119”L x 86”W x 84”H)
Net Weight Approximately 9,520 lbs.
Operational Requirements
ExhaustNone needed
Cycles Per Bottle
Make it possible.
RevoxSterilization.com
© 2016 Mar Cor Purification Inc., A Cantel Medical Company. All Rights Reserved. REVOX,® JUST IN TIME STERILIZATION™ and Make it possible.™ are registered trademarks of Mar Cor Purification Inc., A Cantel Medical Company.
REVOX Sterilization Solutions14605 28th Avenue North
Minneapolis, MN 55447
Make it possible.
Exhaust None needed
Power 460 VAC 3 Phase 20 AMPS
Air 2.6 CFM at 80 PSI
Water 1 GPM
Facility Temperature 18-30°C (65-86°F)
Operational Requirements
Usable Volume 12 cubic ft.
Physical Dimensions 84 cm x 132 cm x 191 cm (33”L x 52”W x 75”H)
Net Weight Approximately 2,000 lbs.
Technical SpecificationsRe
voxS
teril
izat
ion.
com
© 20
15 M
AR CO
RAll R
ights
Rese
rved.
PN XX
XXX-X
XX/A
REVO
X® is
a reg
istere
d trad
emark
of M
AR CO
R,AC
antel
Med
ical C
ompa
ny.
REVO
X St
erili
zati
on S
olut
ions
1460
5 28
th A
venu
e N
orth
Min
neap
olis
, MN
554
47
The REVOX sterilization process utilizes a multi-tote system that safely allows your products, or components, to be loaded into the chamber and sterilized.
Whether it’s utilizing our in-house capacity for your sterile processing needs, or bringing the device into your facility as part of your manufacturing process, the REVOX process can quickly and safely sterilize your critical components and devices.
REVOX 417L
REVOX™ 417L Processing Unit
The REVOX™ sterilization process uses a room temperature, vaporized, peracetic
acid sterilant, which is injected into a variable vacuum sterilization chamber under
controlled conditions. REVOX® Sterilization Solution’s unique process and flexible
operating abilities allow for the routine execution of traditionally difficult to achieve
custom sterilization cycles.
The REVOX Sterilization Solutions utilizes a multi-tote system that safely allows your
products, or components, to be loading into the chamber and sterilized. Whether It’s
utilizing our in house capacity for your sterile processing needs, or bringing the device
into your facility as part of your manufacturing process, REVOX Sterilization Solutions
can quickly and safely sterilize your critical components and/or devices.
The REVOX team is part of the Cantel Medical Inc company (NYSE:CMN); a company dedicated to infection prevention and control.Our team includes mechanical engineers, chemists, microbiologists, quality assurance and regulatory affairs professionals. TheREVOX team will work to understand your challenges, concerns, and opportunities and provide expert insight to help you decideif REVOX is the right sterilization solution for your product or product concept, and/or operational efficiency improvement goals.
www.revoxsterilization.com Call us at 855.473.5690
About REVOX Sterilization Solutions ISO 13485:2003 Compliant Quality System
14605 28th Avenue North Minneapolis, MN 55447Phone: 855.473.5690
2014 MEDIVATORS INC.
All Rights Reserved.
PN: 50098-526/A
Technical Specifications
Usable Volume 12 cubic ft
Overall Chamber Volume 15 cubic ft
Physical Dimensions 33"L X 52"W x 70" H
Net Weight Approximately 1000 lbs
Operational Requirements
Exhaust None needed
Power 230 VAC Single Phase
Air 2.6 CFM at 80 PSI
Water None needed
REVOX Process Consumables*
Liquid Sterilant REVOX PA
Standard Bottle Size 1 qt (0.94L)
Cycles Per Bottle 6-12
Biological IndicatorsSelf-Contained with
G. stearothermophilus andgrowth indicated by color-change
CI REVOX PA CI - Red to Blue
Filter LifeIndicated and Monitored by the REVOX Sterilization Equipment
REVOX® is a registered trademark of Medivators Inc., A Cantel Medical Company.
Standard Features
• Gentle room temperature process (18oC – 30oC)
• No harmful residuals. PAA chemistry breaks down to CO2,
H20, and O2
• No lengthy pre-conditioning or post-processing aeration
required
• Additional multiple unit configuration options for safe,
efficient, on-site processing
• Fast turn-around contract sterilization services
• Expert guidance to help meet technical, operational, and
financial project objectives
• Technical support and on-site maintenance provided by a
nationwide service network.
*All consumables costs are included in agreed upon per run cost. Consumbale levelsare monitored and re-stocked by REVOX Sterilization Solutions automatically.
PNxxxxxx/x