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.
Manufactured by
Izmir, Türkiye
We are continuing our activities in our factory in the Izmir Ataturk Organized Industrial Zone since 1998. As Kordon Tıp, we contribute to our country s economy by bringing out contemporary and modern products with our pioneering and innovative studies. We have domestic and foreign solutions with our dealer network which is in the center of Izmir and our Technical Service with Turkish Standards Institute Service Qualification, Ministry of Industry and Trade, After Sales Service Qualification Certificate. Our Technical Service; Installation and assembly, usage and maintenance training, warranty and non-warranty repair and maintenance services, we can list as spare parts subject. Our Mission To create products with quality and timely delivery principle to meet the expectations of our customers on an international platform. Our Vision To increase the quality of production by carrying our contribution to the health sector to the highest point.
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12 of 55 closest product alternatives
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.
LISTER BIOMEDICAL CO., LTD. · China
Standard biological indicator for steam sterilization processes with 24-hour readout. Provides comprehensive sterilization verification using spore-based monitoring technology.
STERIFAST - STERILIZATION & DISINFECTION SYSTEMS LDA. · Portugal
Biological indicator containing heat-resistant spores for validating steam sterilization cycles. Used to monitor autoclave performance and ensure effective sterilization of medical instruments.
LISTER BIOMEDICAL CO., LTD. · China
Biological indicator designed for low-temperature steam and formaldehyde sterilization processes with 24-hour readout. Validates effectiveness of alternative sterilization methods.
LISTERBIOMEDICAL Co.,LTD · South Korea
A 24-hour biological indicator formulated for low-temperature steam and formaldehyde sterilization processes. Delivers accurate verification of sterilization cycles in sensitive equipment applications.
LISTER BIOMEDICAL CO., LTD. · China
20-minute rapid biological indicator for steam sterilization processes, enabling faster verification of sterilization effectiveness. Supports timely release of sterilized medical equipment in clinical settings.
LISTERBIOMEDICAL Co.,LTD · South Korea
A rapid biological indicator providing sterilization verification results within 10 minutes for steam sterilization processes. Enables quick confirmation of sterilization cycle success in time-sensitive healthcare environments.
Anhui Tianrun Medical Packaging Materials Co. Ltd. · China
A biological indicator for steam sterilization processes providing rapid results in 30 minutes. It enables quick verification of steam sterilization effectiveness for medical devices with faster turnaround compared to standard 24-hour indicators.
Suzhou LOSH Biotechnology Co., Ltd · China
A biological indicator in suspension format used to validate the effectiveness of steam sterilization processes at high pressure and temperature in medical settings.
LISTER BIOMEDICAL CO., LTD. · China
Ultra-rapid biological indicator enabling sterilization verification within 10 minutes for steam processes. Facilitates faster turnaround times in healthcare facilities requiring immediate equipment availability.
Suzhou LOSH Biotechnology Co., Ltd · China
A biological indicator containing heat-resistant spores used to validate the effectiveness of dry heat sterilization processes in laboratory and medical device sterilization.
Andersen Sterilizers · United States
A biological indicator containing spores used to validate the sterilization process of the EOGas 4PLUS system by confirming that sterilization conditions are sufficient to achieve the required sterility assurance level.
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