Historical

ANSI/AAMI/ISO 11135-1:2007

Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices


Establishes requirements for validation and routine control of ethylene oxide sterilization processes for medical devices.


CONTENT PROVIDER
Association for the Advancement of Medical Instrumentation [aami]

Others Also Bought
Sterilization of health care products- Ethylene oxide -Part 2: Guidance on the application of ANSI/AAMI/ISO 11 ...
Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms ...
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems ...
Document History
Revises:
  • Partial revision of ANSI/AAMI/ISO 11135:1994
Included in Packages
This standard is not included in any packages.
Amendments & Corrections
We have no amendments or corrections for this standard.