Class B Autoclave Steam Sterilizer Medical Devices Full Certificate Dentistry Ophthalmology Oral Therapy Equipments Accessories

A Class B autoclave uses a vacuum-assisted steam sterilization process and is capable of sterilizing porous loads, packed instruments, and hollow items. Compared with Class N or Class S units, Class B offers more complete steam penetration and validated cycles for a wider range of medical/dental devices.

This autoclave is designed for dental, ophthalmology and oral therapy instruments, as well as other small medical devices and laboratory tools that require steam sterilization. It supports packaged and unwrapped solid, porous and hollow instruments when used according to validated cycles.

Two physical capacity options are offered: 18L and 23L. The number of instruments depends on their size and packaging; use appropriate trays and do not overload the chamber to ensure proper steam penetration.

The product is CE certified and listed with safety standard GB/T18830-2009. It is classified as a Class II instrument. Always verify local regulatory requirements and retain certification documents for inspection.

The autoclave is electrically powered. Specific voltage, current and frequency requirements are model-dependent; contact online technical support or refer to the user manual for the exact electrical specifications for your region.

Class B autoclaves typically provide vacuum-assisted cycles at validated temperatures (commonly 121°C and 134°C) with drying phases. Exact cycle selections and times are described in the product manual—consult it or technical support for cycle parameters for your model.

Yes. Online technical support is provided by the manufacturer/brand (FZX). For assistance, have your model number (FRRomus), serial number and purchase details ready and contact the supplier’s support channel listed in your documentation or on the product listing.

Regular maintenance includes cleaning the chamber and door gasket, draining and descaling according to water hardness, checking and replacing seals as needed, and following the manufacturer’s preventive maintenance schedule. Keep records of maintenance and service actions.

Use biological indicators (spore tests) and chemical indicators according to local regulations and facility protocol. Run routine Bowie-Dick or equivalent vacuum integrity tests for porous load cycles and document results to ensure ongoing sterilization efficacy.

Included accessories vary by seller. Typical items may include removable trays and basic instrument racks. Sterilization pouches and specialized trays are usually sold separately—confirm the included items with the supplier before purchase.

The listed shelf life in the specification is 1 year. For medical equipment this often refers to recommended storage/use conditions or warranty/consumable guidance—confirm with the supplier whether this relates to warranty, consumable parts or storage recommendations.

The unit is compact (available in 18L and 23L sizes) but requires a stable, level surface, proper ventilation and access to a suitable electrical supply. Follow the installation instructions in the manual and consult technical support for site-specific requirements.

Do not open the door until pressure and temperature have returned to safe levels. Wear appropriate PPE when loading/unloading. Use only recommended water types (demineralized if specified), follow cycle instructions, and ensure instruments are arranged to allow steam penetration.

The unit carries CE certification and meets GB/T18830-2009, but local regulatory acceptance varies. Check with your national/regional health authority or infection control department to confirm that the autoclave meets all applicable regulatory and accreditation requirements for your facility.