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About This Item

 

Full Description

This International Standard specifies the requirements for the safety of nerve and muscle STIMULATORS, defined in subclause 201.3.204, for use in the practice of physical medicine, hereinafter referred to as ME EQUIPMENT. This includes transcutaneous electrical nerve STIMULATORS (TENS) and electrical muscle STIMULATORS (EMS).
 

Document History

  1. CAN/CSA C22.2 No. 60601-2-10:14 (R2023)

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    Medical Electrical Equipment - Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators (Adopted IEC 601- 2-10:1987)

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  2. CAN/CSA C22.2 NO. 601.2.10-92 (R2009)


    Medical Electrical Equipment - Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators (Adopted IEC 601- 2-10:1987)

    • Historical Version
 

Amendments, rulings, supplements, and errata

  1. CAN/CSA C22.2 NO. 60601-2-10:14/A2:23


    Amendment 2:2023 to CAN/CSA-C22.2 NO. 60601-2-10:14, Medical electrical equipment - Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators (Adopted amendment 1:2023 to IEC 60601-2-10:2012)

  2. CAN/CSA C22.2 NO. 60601-2-10A:14 (R2023)


    Amendment 1:2018 to CAN/CSA-C22.2 NO. 60601-2-10:14, Medical electrical equipment - Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators (Adopted amendment 1:2016 to IEC 60601-2-10:2012)