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About This Item

 

Full Description

Specifies general criteria for estimating bioburden on a medical device, raw material or package.

Cross References: EN 550*EN 552*EN 554*EN 556*EN 724*prEN 866-1*prEN 1174-2*prEN 1174-3*prEN 1632*EN 29004*EN 45001*EN 46002*EN ISO 9002*90/385/EEC*93/42/EEC*BS EN ISO 9001*BS EN 46001*
 

Document History

  1. BS EN ISO 11737-1:2018+A1:2021


    Sterilization of health care products. Microbiological methods-Determination of a population of microorganisms on products

    • Most Recent
  2. BS EN ISO 11737-1:2018


    Sterilization of health care products. Microbiological methods-Determination of a population of microorganisms on products

    • Historical Version
  3. BS EN ISO 11737-1:2006


    Sterilization of medical devices. Microbiological methods-Determination of a population of microorganisms on products

    • Historical Version
  4. BS EN 1174-3:1997


    Sterilization of medical devices. Estimation of the population of micro-organisms on product-Guide to the methods for validation of microbiological techniques

    • Historical Version
  5. BS EN 1174-2:1997


    Sterilization of medical devices. Estimation of the population of micro-organisms on product-Guidance

    • Historical Version
  6. BS EN 1174-1:1996

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    Sterilization of medical devices. Estimation of the population of micro-organisms on product-Requirements

    • Historical Version