AIR FILTER
GVS Respiratory line include a proprietary range of HME (Heat and Moisture Exchanger) and HMEFs (Heat and Moisture Exchanger and bacterial / viral Filter) and Filters (Bacterial and Viral) for use in anesthesia, intensive therapy, respiratory medicine, and ventilation, with efficiencies up to 99.99999%. A series of insufflation products for use during laparoscopic surgery have more recently been added to the range. This GVS Filters section provides an overview of the products relevant to each category, e.g. Filters, HME, HMEFs, Suction Filters, Insufflation Filters, Spirometry, Vent Filters, and Homecare.
Technical product specifications provides detailed information on performance: e.g. efficiency, resistance to flow, moisture output (if applicable), dead-space, weight, connector size and overall dimensions.
Please note that products are available bulk packed, individually packed clinically clean, and or individually sterile upon request.
GVS Respiratory line products are designed and manufactured using quality systems in accordance with BS EN ISO 9001:2008, BS EN ISO 13485:2003 and to the Medical Devices Directive 93/42 EEC. This means that Air Safety has the CE Marking on all class IIa filters. Sterile filters are EtO Sterilised to ISO11135-1 and Sterility Assurance Level (SAL) monitoring is based on ISO 11737-1 re-Microbiological Methods.
GVS Respiratory line include a proprietary range of HME (Heat and Moisture Exchanger) and HMEFs (Heat and Moisture Exchanger and bacterial / viral Filter) and Filters (Bacterial and Viral) for use in anesthesia, intensive therapy, respiratory medicine, and ventilation, with efficiencies up to 99.99999%. A series of insufflation products for use during laparoscopic surgery have more recently been added to the range. This GVS Filters section provides an overview of the products relevant to each category, e.g. Filters, HME, HMEFs, Suction Filters, Insufflation Filters, Spirometry, Vent Filters, and Homecare.
Technical product specifications provides detailed information on performance: e.g. efficiency, resistance to flow, moisture output (if applicable), dead-space, weight, connector size and overall dimensions.
Please note that products are available bulk packed, individually packed clinically clean, and or individually sterile upon request.
GVS Respiratory line products are designed and manufactured using quality systems in accordance with BS EN ISO 9001:2008, BS EN ISO 13485:2003 and to the Medical Devices Directive 93/42 EEC. This means that Air Safety has the CE Marking on all class IIa filters. Sterile filters are EtO Sterilised to ISO11135-1 and Sterility Assurance Level (SAL) monitoring is based on ISO 11737-1 re-Microbiological Methods.
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