EN 60601-2-22:2013

Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment

Publication date:   Feb 15, 2013

General information

99.60 Withdrawal effective   Oct 30, 2023

CENELEC

CLC/TC 76 Optical radiation safety and laser equipment

European Norm

11.040.01   Medical equipment in general | 31.260   Optoelectronics. Laser equipment

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Scope

Applies to the basic safety and essential performance of laser equipment for either surgical, therapeutic, medical diagnostic, cosmetic, or veterinary applications, intended for its use on humans or animals, classified as a class 3B or class 4 laser product as defined by 3.22 and 3.23 in IEC 60825-1, hereafter referred to as laser equipment. Throughout this International Standard, light emitting diodes (LED) are included whenever the word 'laser' is used. This standard can also be applied to surgical, cosmetic, therapeutic and diagnostic laser equipment used for compensation or alleviation of disease, injury or disability. This third edition cancels and replaces the second edition of IEC 60601-2-22, published in 1995. This edition constitutes a technical revision. This third edition takes account of the recently published new editions of the General Standard IEC 60601-1 and Group safety publication IEC 60825-1. Additionally, it addresses technical and safety issues which have arisen in the time following the previous second edition.

Related legislation

Legislation related to this standard

93/42/EEC

Medical devices

Life cycle

PREVIOUSLY

WITHDRAWN
EN 60601-2-22:1996

NOW

WITHDRAWN
EN 60601-2-22:2013
99.60 Withdrawal effective
Oct 30, 2023

REVISED BY

PUBLISHED
EN IEC 60601-2-22:2020