Standard chemical indicator test pack used to validate steam sterilizer performance and steam penetration into medical device packages. Required for routine autoclave quality assurance testing.
Manufactured by
Boticas, Portugal
Sterifast Lda. is a leading company in Low Temperature Hydrogen Peroxide Sterilization Systems (Low Concentration). Our ECOPlasma system uses only 35% H202 concentration and it is designed to sterilize medical devices in general and thermo-sensitive medical devices. The ECOPlasma process with much lower concentration allows the shipment of the sterilizing agent by air. The process and device are protected by the patent PCT/PT2007 /000029 with international publication number W02009008755 A 1. We offer to our clients complete and customized medical packaging solutions. AII products have always been subjected to strict quality inspections and our team applies for continuous improvement and compliance of applicable standards and requirements. STERIFAST is on its way to stop infection and improve the performance of the bacterial barrier, while still saving on costs. We also present our calibration and QC laboratories for autoclave validation. STERIFAST is a Known Consignor for air cargo (PT/KC/0006-01)
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STERIVIC MEDICAL CO.,LTD · China
A Bowie-Dick test pack used to evaluate the penetration and effectiveness of steam sterilization processes. This standard test pack contains a chemical indicator and is used for routine steam sterilizer validation and quality assurance.
Shanghai Jianzhong Medical Packaging Co., Ltd. · China
A chemical indicator used for sterilization monitoring to verify that sterilization conditions have been achieved in medical device packaging.
ANQING BAOJIE PACKAGING CO., LTD · China
Chemical indicator cards that change color in response to steam sterilization exposure, validating that appropriate temperature, pressure, and time conditions have been met. These cards are routinely placed in sterilization packages for process monitoring.
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A rapid biological indicator for steam sterilization validation that offers quick turnaround results. It contains bacterial spores to confirm the effectiveness of steam sterilization in medical device processing.
Kordon Tip Saglik Arac ve Gerecleri Mühendislik Proje Ithalat San. ve Tic Ltd. Sti. · Türkiye
Rapid biological indicator designed for steam sterilization validation and monitoring. Provides quick assessment of sterilization efficacy in autoclave processes.
LISTERBIOMEDICAL Co.,LTD · South Korea
A 24-hour biological indicator designed to verify steam sterilization processes by monitoring spore destruction. Used in healthcare facilities to validate sterilization cycle effectiveness and ensure patient safety.
Reverberi srl · Italy
A standard biological indicator test for steam sterilization validation in dental laboratory autoclaves.
Kordon Tip Saglik Arac ve Gerecleri Mühendislik Proje Ithalat San. ve Tic Ltd. Sti. · Türkiye
A rapid biological indicator designed for steam sterilization processes that provides faster incubation results. It is used to validate the efficacy of steam sterilization procedures in medical device and equipment sterilization.
Kordon Tip Saglik Arac ve Gerecleri Mühendislik Proje Ithalat San. ve Tic Ltd. Sti. · Türkiye
A biological indicator used for steam sterilization validation with a 24-hour incubation period. It contains bacterial spores to monitor and verify the effectiveness of steam sterilization in medical equipment and device processing.
Nantong Fuhua Packing Co., Ltd. · China
A biological indicator test pack used to validate sterilization processes and ensure the effectiveness of sterilization equipment in medical facilities.
LISTERBIOMEDICAL Co.,LTD · South Korea
A standard Bowie Dick test pack designed to evaluate steam penetration in autoclave sterilizers. Used to verify proper steam circulation and pressure during sterilization cycles.
VICTORIS HEALTH · Türkiye
Chemical indicators used to test the penetration and effectiveness of steam sterilization processes. These tests help verify proper steam penetration in porous loads and validate sterilizer performance.
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