Sterilization Compatibility Table for Medical Packaging Materials
EO/FORM (at least a part of the packaging needs to be permeable to gas)
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Plastics Compatibility with Sterilization Methods
Polymer Category Polymer Abbreviation Autoclave Dry Heat Ethylene Oxide (EtO) Gamma Irradiation Electron Beam Biopolymers Poly(L-lactide) PLLA Fair Good Good
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Medical Device Sterilization Methods Comparison
Penetrates packaging materials and device lumens. Optimal material compatibility (Low temp). “Product can be sterilized in its sealed final packaging.” Simple operation and monitoring. Broad microbicidal activity. Low temperature. Sterility assurance and therapeutic effect. Allows immediate product release after processing (Parametric Release), shortening turnaround time, helping to get products to market quickly. Customizable number of single-use disinfectable products. Always meets product and regulatory requirements.
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Ethylene Oxide (EtO) Emissions Control: Technologies and Solutions
Effective EtO emissions control is essential for sterilization, chemical manufacturing, and industrial operations handling ethylene oxide (EtO). Modern abatement technologies help facilities meet regulatory requirements, improve safety, and minimize environmental impact. This guide provides an optimized, SEO-ready overview of primary EtO control technologies, including wet scrubbers, thermal oxidizers, dry bed scrubbers, catalytic oxidizers, flares, bubbling scrubbers, and integration considerations.
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How to Test ETO Gas Sterilization Test Materials
When it comes to ETO gas sterilization, testing is an essential part of ensuring the effectiveness and safety of the sterilization process. ETO GAS STERILIZATION TEST MATERIALS
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ETO STERILIZATION Safety Guidelines: Best Practices for Using Ethylene Oxide as a Sterilant
Ethylene oxide (ETO STERILIZATION) is widely used as a low-temperature sterilant in industries like healthcare, pharmaceuticals, and biotechnology. However, due
Common Ethylene Oxide (EO) Sterilization Non-Conformities in Medical Device Manufacturing
IntroductionEthylene Oxide (EO) sterilization remains a preferred method for medical devices incompatible with radiation or moist heat. However, it’s a
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ETO Sterilization Re-qualification
ETO Sterilization Re-qualification Requirements 1. Re-qualification Frequency • Minimum annual requirement• At least once per year, verification data, subsequent re-validation data,
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Performance Qualification(pq)-ppq in eo sterilization
Physical Performance Qualification (PPQ)• It shall be demonstrated that all specified acceptance criteria are reproducible throughout the entire process.How many
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