AES-CERBERUS™ is a class I Medical device which complies with EN 16442:2015 and Medical Device Regulation 2017/745. Its system is patented and validated with cold plasma technology for the elimination of pathogens. An innovative solution which guarantees the maximum protection of enveloped material that needs to be transported and stored under aseptic conditions.
The device involves the usage of dedicated CERBERUS-BAG™ bags sterilized through gamma ray technology, which can be used to transport both disinfected instruments and contaminated ones returning from the reprocessing area.
The machine employs vacuum technology alternated with “cold plasma” injections with generation of free radicals (mdg patent).
At the end of the process the instrument is sealed inside of the bag through heat-sealing to ensure aseptic conditions up to 800 hours.
AES-CERBERUS™ was created both to centralize the conservation process and to facilitate daily usage in high and low workflow wards, such as the departments of endoscopy, ENT, bronchoscopy, urology, intensive care and cardiology (for TEE probes).
Designed to be compatible with every brand and model of endoscope, transesophageal probe (TEE) and other medical devices subject to high-level disinfection, without the need for connections to the endoscope channels.