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About This Item

 

Full Description

1.1 Scope

Addition:

This Particular International Standard applies to LASER EQUIPMENT FOR MEDICAL APPLICATIONS, as defined in 2.1.111 classified as a CLASS 3B or 4 LASER PRODUCT according to 3.17 and 3.18 in IEC 825-1, hereinafter referred to as LASER EQUIPMENT.

NOTE - LASER EQUIPMENT for medical applications classified as a CLASS 1, 2 or CLASS 3A LASER PRODUCT, is covered by IEC 601-1 and IEC 825-1.

1.2 Object

The object of this Particular Standard is to specify particular requirements for the safety of LASER EQUIPMENT for medical applications classified as a CLASS 3B or CLASS 4 LASER PRODUCT.

 

Document History

  1. CAN/CSA C22.2 NO. 60601-2-22:23


    Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment (Adopted IEC 60601-2-22:2019, fourth edition, 2019-11, with Canadian deviations)

    • Most Recent
  2. CAN/CSA C22.2 NO. 60601-2-22-08 (R2018)


    Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment (Adopted IEC 60601-2-22:2007, third edition, 2007-05)

    • Historical Version
  3. CAN/CSA C22.2 NO. 60601-2-22-01 (R05)

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    Medical Electrical Equipment - Part 2: Particular Requirements for the Safety of Diagnostic and Therapeutic Laser Equipment (Adopted CEI/IEC 601-2-22:1995, second edition, 1995-11)

    • Historical Version