ETO Sterilization Validation Regulatory Requirements

ETO Sterilization Validation Regulatory Requirements

Ensuring full compliance with international standards is the cornerstone of Oxyde d'éthylène (ETO) Stérilisation. Validation procedures must follow a rigorous framework to guarantee medical device safety and efficacy. Below is the comprehensive list of ETO Sterilization Regulatory Requirements and ISO standards that govern the industry today.

01
OIN 11135: 2014 Sterilization of health-care products — Ethylene oxide — Requirements for development, validation and routine control of a sterilization process.
02
EN 1422: 2014 Sterilizers for medical purposes — Ethylene oxide sterilizers — Requirements and test methods.
03
OIN 13485 Medical devices — Quality management systems — Requirements for regulatory purposes.
04
OIN 11138-2: 2017 Sterilization of health care products — Biological indicators — Part 2: Biological indicators for ethylene oxide sterilization processes.
05
OIN 10993-7: 2008 Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals.
06
AAMI TIR28: 2016 Product adoption and process equivalence for ethylene oxide sterilization.
07
AAMI TIR16: 2017 Microbiological aspects of ethylene oxide sterilization.
08
OIN 11139: 2018 Sterilization of health care products — Vocabulary of terms used in sterilization standards.
09
OIN 11737-1: 2006 Sterilization of medical devices — Microbiological methods — Part 1: Determination of a population of microorganisms on products.
10
OIN 14937: 2009 General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process.

BOCON’s Commitment to Compliance

Navigating the complex landscape of ETO Sterilization Regulatory Requirements can be challenging. BOCON equipment is designed to meet and exceed these global ISO and AAMI standards, ensuring that your sterilization facility passes every audit with confidence. From OIN 11135 validation support to residual analysis guidance (OIN 10993-7), our team is here to support your compliance journey.

Need Technical Support for ETO Validation?

Get professional consultation on ISO 11135 et FR 1422 compliance for your sterilization facility.

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