C16CC8872C404F62F94158B29124F888
C16CC8872C404F62F94158B29124F888
6CA0D5F7F253ACA75939F14CC38D4221

STEAMPlus™ Class 5 Sterilization Integrator Strips Box of 100

$58.79

In Stock in PA, FL, IN, TX, NV

SPS Medical # SSI-100

Benco Product # 3095-107

Product Line: 1305A - ASEPSIS - STERILE TESTS & INDICATORS

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Product Details

The STEAMPlus Sterilization Integrator is an “advanced technology” medical device that provides a simple, accurate method of assuring that proper conditions for sterilization have been met during a sterilizer cycle. For use with all Steam processes (gravity, prevacuum and flash), the STEAMPlus has documented performance equivalent to a biological indicator. The STEAMPlus Sterilization Integrator is engineered to integrate the three (3) critical variables of sterilization: time, temperature, and saturated steam. This information is displayed in a precise, easy-to-read format. When the dark bar enters the blue SAFE area, sterilization criteria has been met. If the dark bar does not reach the blue SAFE area, proper conditions for sterilization have not been achieved and the processed load should not be released. The STEAMPlus Sterilization Integrator has been tested to the AAMI ST-60 and ISO 11140-1:2005 standards performance requirements. Note: The FDA does not recognize Class 3, 4 or 5 indicators as defined in ISO 11140-1:2005. How to Use the STEAMPlus™ Steam Sterilization Integrator 1. Place a STEAMPlus Integrator (at least once daily) inside a load (i.e. middle of the load or inside the densest pack). A STEAMPlus Integrator should be used in every load containing an implantable device. 2. Process the load according to the sterilizer manufacturer’s instructions. 3. Release the load if the dark bar on the STEAMPlus Integrator has entered the blue SAFE area. If the dark bar has not entered into the blue SAFE area, DO NOT release the load. Storage: Controlled room temperature. The STEAMPlus Integrator is not to replace the weekly use of a biological indicator, but instead is intended to give users immediate notification of whether all critical parameters of steam sterilization have been met. This knowledge is intended to help reduce the release of non-sterile items.

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