Case Medical Receives FDA Marketing Clearance for SteriTite System
Case Medical, Inc. announces it has received FDA 510k clearance for its SteriTite sealed container system and MediTray products for use in the STERIS Amsco V-PRO 1 low temperature sterilization system.
Case Medical was previously cleared for pre-vacuum and gravity steam sterilization, EtO, STERRAD 100, 100S, 200, NX and sealed flash using its FlashTite valve plate, TSO3 ozone 125L, and pre vacuum flash sterilization using the disposable filter.
Case Medical’s SteriTite container system is ideal for standardization as the same container is fully compatible and validated with all current sterilization methods. Furthermore, the SteriTite container system meets sterilizer manufacturers’ recommendations for processing of surfaces as well as lumens, including rigid and flexible endoscopes.
Recently relocated to a larger state-of-the-art facility in South Hackensack, N.J., Case Medical, Inc. has doubled its manufacturing capability. An acknowledged innovator and custom manufacturer, Case Medical, is committed to developing, manufacturing and implementing the industry’s safest and most effective sterilization systems.
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