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ISO 11137:1995

Withdrawn Date published:

Warning: Withdrawn Standard. This document has been withdrawn without replacement. You may wish to search for a more up to date equivalent.

Sterilization of health care products — Requirements for validation and routine control — Radiation sterilization

Specifies requirements for validation, process control and routine monitoring in the radiation sterilization of health care products. Applies to continuous and batch type gamma irradiators using the radionuclides 60 Co and 137 Cs, and to irradiators using a beam from an electron or x-ray generator. Does not cover facility design, licensing, operator training, factors related to radiation safety, the assessment of the suitability of the product for its intended use.

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Related Information

Similar Standards

  • AS/NZS ISO 11137.1:2006

    Sterilization of health care products - Radiation - Requirements for development, validation and routine control of a sterilization process for medical devices

  • AS/NZS ISO 11137.3:2006

    Sterilization of health care products - Radiation - Guidance on dosimetric aspects

  • BS EN 556-1:2024

    Sterilization of medical devices. Requirements for medical devices to be designated "STERILE", Requirements for terminally sterilized medical devices

  • BS EN 556-1:2024 - TC

    Tracked Changes. Sterilization of medical devices. Requirements for medical devices to be designated "STERILE", Requirements for terminally sterilized medical devices

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ISO 11137:1995

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