Sterilization

hasnt changed
in decades.
Were making up
for lost time.

Make it possible.

What Is
REVOX Sterilization Solutions?
REVOX Sterilization Solutions provides expert guidance and services
to meet the most ambitious project objectives related to terminal
sterilization; from increasing manufacturing efficiency to achieving optimal
sterilization outcomes for complex or delicate devices or materials.
The REVOX sterilization technology uses room temperature vaporized
peracetic acid (VPA), which is injected into a pressurized chamber. Room
temperature VPA greatly improves material compatibility over other
sterilization methods that incorporate heat. In fact, in May 2014 medical
manufacturer OsteoSymbionics announced that it had received FDA 510(k)
clearance for its Class II CLEARSHIELD cranial implant, using the REVOX
sterilization technology.
REVOX Sterilization Solutions offers:
Feasibility and Validation Testing
Contract or On-Site Sterilization Options
RevoxSterilization.com

Chamber size options to meet throughput needs

Expert guidance to help meet technical, operational,
regulatory, and financial project objectives

Room Temperature Sterilization.

REVOX Makes It Possible.
Superior materials compatibility
with ultra-low residuals
Safe on-site processing vapor breaks down
to water, carbon dioxide, and oxygen v. known
carcinogens for ethylene oxide (EO)
Lower sterilization temperature
compared to common sterilization
alternatives (18C - 30C)
Fast turnaround time with no
pre or post-aeration
More packaging options
Better operational flexibility and per-unit
cost efficiency

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From Biologics To Electronics And Beyond.

Unleash Your Potential.
Until now, youve been limited by traditional sterilization methods that constrain your choice
of materials and overall product design. REVOX changes that. Incorporating a proprietary
VPA sterilization method and true room temperature processing, REVOX is compatible
with the vast majority of materials used in medical devices and packaging. This superior
compatibility enables you to innovate more efficiently and create the products that will
demonstrate your true potential.

KEY
BENEFITS

Testing has verified compatibility with over 100 different materials,* including
thermoplastics, thermosets, adhesives, elastomers, metals, ceramics, and glass
The REVOX team continues to test new materials every day
Safely sterilize devices with electronic
components and batteries

Compatible with biomed materials, tissues,

and bio-absorbable products
*Ask your REVOX consultant for a complete material compatibility list.

Just-In-Time Sterilization.
Its About Time.
REVOX continues to offer off-site sterilization at our facilities, as an option for
manufacturers who need to sterilize small-run quantities or products in the R&D phase.
However, for manufacturers with larger-volume, recurring production cycles, adding REVOX
sterilization directly into in-house processing offers greater efficiency and a significant
reduction in production costs, including logistical expenses. The potential for an on-site,
in-line sterilization process using REVOX sterilization offers several key benefits, including:
Increased throughput
Easy to integrate
Reduced inventory levels
Greater quality control
Shorter turnaround time for greater manufacturing efficiency
Reduced customer lead times
JUST IN TIME sterilization
Limited capital investment
To safely and easily integrate scalable in-line sterilization into your manufacturing
process, its almost as simple as plugging in the machineno exhaust or other
special infrastructure is needed. Adding REVOX to your production line speeds up
your production and gives you a substantial competitive edge. Plus, REVOX machines
are available in 417L and 3,000L capacity options, so that batch processing can be
customized to your unique production cycle.
REVOX 417L

REVOX 3000L

Technical Specification

Technical Specification
12 cubic ft.

Usable Volume

Usable Volume

96 cubic ft.

Physical Dimensions

84 cm 132 cm 191 cm
(33"L 52"W 75"H)

Physical Dimensions

302 cm 218 cm 213 cm

(119"L 86"W 84"H)

Net Weight

Approximately 2,000 lbs.

Net Weight

Approximately 9,520 lbs.

Operational Requirements
Exhaust
Power
Air
Water
Facility Temperature

Operational Requirements
None needed

460 VAC 3 Phase 20 AMPS

2.6 CFM at 80 PSI
1 GPM
1830C (6586F)

RevoxSterilization.com
2016 Mar Cor Purification Inc. All Rights Reserved. PN 3031229/A
REVOX is a registered trademark of Mar Cor Purification Inc. A Cantel Medical Company.
CLEARSHIELD is a registered trademark of OsteoSymbionics.

Exhaust
Power
Air
Water
Facility Temperature

None needed
Two 460 VAC 3 Phase 20
16 CFM at 90 PSI
2 GPM
1830C (6586F)

REVOX Sterilization Solutions

14605 28th Avenue North
Minneapolis, MN 55447