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MAR
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REVO
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Make it possible.
Just-In-Time Sterilization.™
It’s about time.
REVOXTM 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.
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 Specifications
Revo
xSte
riliz
atio
n.co
m©
2015
MAR
COR A
ll Righ
ts Re
serve
d. PN
XXXX
X-XXX
/A RE
VOX®
is a
regist
ered t
radem
ark of
MAR
COR,
A Can
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
The REVOXTM 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, REVOXTM can quickly and safely sterilize your critical components and devices.
REVOXTM 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. The REVOX team will work to understand your challenges, concerns, and opportunities and provide expert insight to help you decide if 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 and growth 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 levels are monitored and re-stocked by REVOX Sterilization Solutions automatically.
© 2016 Mar Cor Purification Inc., A Cantel Medical Company. All Rights Reserved. PN3028923/A REVOX,® JUST IN TIME STERILIZATIONTM and Make it possible.™ are registered trademarks of Mar Cor Purification Inc., A Cantel Medical Company.
RevoxSterilization.com
REVOX Sterilization Solutions14605 28th Avenue North
Minneapolis, MN 55447