IEC 60601-2-22:2007 ED3

Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment IEC 60601-2-22:2007 ED3

Publication date:   May 23, 2007

General information

99.60 Withdrawal effective   Nov 20, 2019

WPUB   

IEC

TC 76

International Standard

11.040.50   Radiographic equipment | 11.040.60   Therapy equipment | 31.260   Optoelectronics. Laser equipment

Buying

Revised

Language in which you want to receive the document.

Scope

Applies to the 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 publication IEC 60825-1. Additionally, it addresses technical and safety issues which have arisen in the time following the previous second edition.

Life cycle

PREVIOUSLY

WITHDRAWN
IEC 60601-2-22:1995 ED2

NOW

WITHDRAWN
IEC 60601-2-22:2007 ED3
99.60 Withdrawal effective
Nov 20, 2019

CORRIGENDA / AMENDMENTS

WITHDRAWN
IEC 60601-2-22:2007/AMD1:2012 ED3

REVISED BY

PUBLISHED
IEC 60601-2-22:2019 ED4