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ISO 24998 FRENCH

Matériel de laboratoire en matière plastique - Boîtes de Petri à usage unique pour méthodes microbiologiques

active, Most Current
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Organization: ISO
Publication Date: 15 November 2008
Status: active
Page Count: 16
ICS Code (Laboratory medicine in general): 11.100.01
ICS Code (Other rubber and plastics products): 83.140.99

Document History

ISO 24998 FRENCH
November 15, 2008
Matériel de laboratoire en matière plastique - Boîtes de Petri à usage unique pour méthodes microbiologiques
A description is not available for this item.

References

This document references:
ISO 11137-1 - Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices AMENDMENT 2: Revision to 4.3.4 and 11.2
Published by ISO on November 1, 2018
A description is not available for this item.
This document references:
ISO 14644-1 - Cleanrooms and associated controlled environments - Part 1: Classification of air cleanliness by particle concentration
Published by ISO on December 15, 2015
This part of ISO 14644 specifies the classification of air cleanliness in terms of concentration of airborne particles in cleanrooms and clean zones; and separative devices as defined in ISO 14644-7....
This document references:
ISO 14644-2 - Cleanrooms and associated controlled environments - Part 2: Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration
Published by ISO on December 15, 2015
This part of ISO 14644 specifies minimum requirements for a monitoring plan for cleanroom or clean zone performance related to air cleanliness by particle concentration, based upon parameters that...
This document references:
ISO 14644-3 - Cleanrooms and associated controlled environments — Part 3: Test methods
Published by ISO on August 1, 2019
This document provides test methods in support of the operation for cleanrooms and clean zones to meet air cleanliness classification, other cleanliness attributes and related controlled conditions....
This document references:
14644-4 - Cleanrooms and associated controlled environments — Part 4: Design, construction and start-up
Published by ISO on November 1, 2022
This document specifies the process for creating a cleanroom from requirements through to its design, construction and start-up. It applies to new, refurbished and modified cleanroom installations....
This document references:
ISO 14644-5 - Cleanrooms and associated controlled environments Part 5: Operations
Published by ISO on August 15, 2004
This part of ISO 14644 specifies basic requirements for cleanroom operations. It is intended for those planning to use and operate a cleanroom. Aspects of safety that have no direct bearing on...
This document references:
ISO 14644-7 - Cleanrooms and associated controlled environments Part 7: Separative devices (clean air hoods, gloveboxes, isolators and mini-environments)
Published by ISO on October 1, 2004
This part of ISO 14644 specifies the minimum requirements for the design, construction, installation, test and approval of separative devices, in those respects where they differ from cleanrooms as...
This document references:
14644-8 - Cleanrooms and associated controlled environments — Part 8: Assessment of air cleanliness by chemical concentration (ACC)
Published by ISO on June 1, 2022
This document establishes typical assessment processes to determine grading levels of air chemical cleanliness (ACC) in cleanrooms and associated controlled environments, in terms of airborne...
This document references:
ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by ISO on August 15, 2006
Inclusions This part of ISO 17665 specifies requirements for the development, validation and routine control of a moist heat sterilization process for medical devices. NOTE Although the scope of this...
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