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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

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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