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Full Description

This standard sets out requirements for designing, manufacturing, marking, testing, selecting and using means of containment for the transportation of Category A and Category B infectious substances in Class 6.2 and clinical, (bio) medical or regulated medical waste.

This standard consists of three parts and one annex.

Part I contains the requirements for the design, test and manufacture of means of containment for infectious substances of Category A and Category B.

Part II contains the requirements for the selection and use of means of containment for infectious substances of Category A and Category B.

Part III contains the requirements for the selection and use of standardized and non-standardized means of containment for the transport of Category A and Category B infectious substances intended for disposal as well as clinical, (bio) medical or regulated medical waste.

Annex A contains the minimum requirements for the completion of a type P620 packagings test report submitted to the Director.
 

Document History

  1. CAN/CGSB 43.125-2016

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    Packaging of Category A and Category B infectious substances (Class 6.2) and clinical, (bio) medical or regulated medical waste

    • Most Recent
  2. CAN/CGSB 43.125-2003


    Design and Manufacture of Packaging for the Transportation of Infectious Substances, Diagnostic Specimens, Biological Products or (Bio) Medical Waste

    • Historical Version
  3. CAN/CGSB 43.125-99


    Packaging of Infectious Substances, Diagnostic Specimens, Biological Products and Biomedical Waste for Transport

    • Historical Version