Advance Pro

For maximum flexibility, FlexiRack can accommodate up to 20 different tray configurations and can be adapted to accept a wide range of loads. Improved drying performance is provided by the autoclave’s HTS (Heat Transfer System), designed to take full advantage of the high performance thermal conductivity properties of aluminium.
Advance Pro also comes with a six colour Visual System Indicator (VSI) giving immediate cycle status and operator peace of mind, together with a selection of water feed and drain options to best meet your needs. The clear, backlit LCD display with simple user friendly 6 push button control system ensures safe and correct operation.

Advance Pro is easy to use, reliable and cost-effective, it’s out-standing performance comes from having over 30 years of high quality autoclave design experience.

Advance Pro is a Class B sterilizer available in 16 or 22 litre capacity units, and all units are fully supported by Prestige Medical’s award-winning customer service and technical service support.

Advance Pro provides Class B vacuum and Class N non-vacuum cycles in the same unit, with a host of new features to help simplify and streamline the day to day sterilization of re-usable medical instruments.

Request a Quote

The Advance Pro has given us peace of mind when we have been short of PPE as we have been able to decontaminate our masks which are normally disposable. This has been instrumental in keeping our patients and staff safe.

Michael O'Brien, MD.

Compliant to international standards and guidelines
• 93/42/EEC Medical Device Directive (MDD)
• 97/23/EEC Pressure Equipment Directive (PED)
• 2012/19/EU Waste Electrical and Electronic Equipment (WEEE)
• BS EN 13060: 2014 Small steam sterilizers
• BS EN 61010-1:2010 Safety requirements for electrical equipment for
measurement, control, and laboratory use
• BS EN 61010-2-040:2015 Safety requirements for electrical equipment for
measurement, control, and laboratory use
• BS EN 61326-1:2013 Electrical equipment for measurement, control and
laboratory use. EMC requirements
• HTM 01-05
• ISO 13485 and ISO 9001
• Restriction of Certain Hazardous Substances in Electrical and Electronic
Equipment Directive under 2011/65/EU
• EN ISO 14971:2012 Risk management for Medical Devices