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IEC

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

(Amendment)

Amendment 1 - Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment

Amendment 1 - Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment

Amendement 1 - Appareils électromédicaux - Partie 2-22: Règles particulières pour la sécurité de base et les performances essentielles des appareils chirurgicaux, esthétiques, thérapeutiques et de diagnostic à laser

General Information

Status
Published
Publication Date
24-Oct-2012
ICS
11.040.50 - Radiographic equipment
11.040.60 - Therapy equipment
31.260 - Optoelectronics. Laser equipment
Technical Committee
TC 76 - Optical radiation safety and laser equipment
Drafting Committee
WG 4 - TC 76/WG 4
Current Stage
DELPUB - Deleted Publication
Completion Date
20-Nov-2019
Ref Project

Relations

Amends
IEC 60601-2-22:2007 - Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment
Effective Date
05-Sep-2023
Revised
IEC 60601-2-22:2019 - Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment
Effective Date
05-Sep-2023

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IEC 60601-2-22:2007/AMD1:2012 - Amendment 1 - Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment Released:10/25/2012IEC 60601-2-22:2007/AMD1:2012 - Amendment 1 - Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment Released:10/25/2012
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IEC 60601-2-22:2007/AMD1:2012 - Amendment 1 - Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment Released:10/25/2012
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IEC 60601-2-22 ®
Edition 3.0 2012-10
INTERNATIONAL
STANDARD
NORME
INTERNATIONALE
AMENDMENT 1
AMENDEMENT 1
Medical electrical equipment –
Part 2-22: Particular requirements for basic safety and essential performance of
surgical, cosmetic, therapeutic and diagnostic laser equipment

Appareils électromédicaux –
Partie 2-22: Règles particulières pour la sécurité de base et les performances
essentielles des appareils chirurgicaux, esthétiques, thérapeutiques et de
diagnostic à laser
IEC 60601-2-22:2007/A1:2012
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IEC 60601-2-22 ®
Edition 3.0 2012-10
INTERNATIONAL
STANDARD
NORME
INTERNATIONALE
AMENDMENT 1
AMENDEMENT 1
Medical electrical equipment –

Part 2-22: Particular requirements for basic safety and essential performance of

surgical, cosmetic, therapeutic and diagnostic laser equipment

Appareils électromédicaux –
Partie 2-22: Règles particulières pour la sécurité de base et les performances

essentielles des appareils chirurgicaux, esthétiques, thérapeutiques et de

diagnostic à laser
INTERNATIONAL
ELECTROTECHNICAL
COMMISSION
COMMISSION
ELECTROTECHNIQUE
PRICE CODE
INTERNATIONALE
CODE PRIX C
ICS 11.040.01, 31.260 ISBN 978-2-83220-418-4

– 2 – 60601-2-22 Amend. 1 © IEC:2012

FOREWORD
This amendment has been prepared by IEC technical committee 76: Optical radiation safety

and laser equipment.
The text of this amendment is based on the following documents:

CDV Report on voting
76/444/CDV 76/477/RVC
Full information on the voting for the approval of this amendment can be found in the report
on voting indicated in the above table.
The committee has decided that the contents of this amendment and the base publication will
remain unchanged until the stability date indicated on the IEC web site under
"http://webstore.iec.ch" in the data related to the specific publication. At this date, the
publication will be
• reconfirmed,
• withdrawn,
• replaced by a revised edition, or
• amended.
NOTE The attention of National Committees is drawn to the fact that equipment manufacturers and testing
organizations may need a transitional period following publication of a new, amended or revised IEC publication in
which to make products in accordance with the new requirements and to equip themselves for conducting new or
revised tests.
It is the recommendation of the committee that the content of this publication be adopted for implementation
...

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