IEC 60601-2-37:2024

Title
Abstract

IEC 60601-2-37:2024 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ULTRASONIC DIAGNOSTIC EQUIPMENT as defined in 201.3.217, hereinafter referred to as ME EQUIPMENT. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant. HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this document are not covered by specific requirements in this document except in 201.7.2.13. This document does not cover ultrasonic therapeutic equipment. Equipment used for the imaging or diagnosis of body structures by ultrasound in conjunction with other medical procedures is covered. IEC 60601-2-37:2024 cancels and replaces the second edition published in 2007 and Amendment 1:2015. This edition constitutes a technical revision.
This edition includes the following significant technical changes with respect to the previous edition:
a) technical and editorial changes resulting from the amended general standard IEC 60601 1:2005, IEC 60601-1:2005/AMD1:2012 and IEC 60601-1:2005/AMD2:2020 and its collateral standards IEC 60601-1-xx,
b) technical and editorial changes as a result of maintenance to normative references;
c) technical and editorial changes resulting from relevant developments in TC 87 Ultrasonics standards. In particular, Clause 201.11 about protection against excessive temperatures and other hazards has been fully revised.

Issue Date

2024-07-02

Category

MED

Included in IECEE System

2024-07-16

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DISCLAIMER: National differences

The National differences and Group differences, National Deviations and Special National conditions (SNC), are based solely on information provided to the Secretariat by the IECEE Member Bodies and/or NCBs and other sources. The IEC/IECEE is not responsible for, nor will it take any position related to, the accuracy or validity of the information provided. To verify the current status of this type of information, we recommend contacting the Member Body (MB) or National Certification Body (NCB) of the relevant country.

Group Differences are applicable for CENELEC member countries: Austria, Belgium, Bulgaria, Croatia, Cyprus, the Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom.

Group/Country

Reference

Last Modified

Differences

TRF Addendum

JapanJapan

2025-02-13

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Laboratory Name

City

Country

Responsible National Certification Body

Suwon-si

Korea, Republic of

Arnhem

Netherlands

Guangzhou

China

Gyeonggi-do

Korea, Republic of

Tokyo

Japan

Shanghai

China

Guangzhou, Guangdong

China

Gyeonggi-do

Korea, Republic of

TRAPPES

France

Gyeonggi-do

Korea, Republic of

Puchheim

Germany

Yokohama

Japan

Shanghai

China

Guangzhou

China

Shenzhen

China

Seoul, 07298

Korea, Republic of

Pleasanton,

United States of America

GORMLEY L0H 1G0

Canada

München

Germany

Ballerup

Denmark

Uiwang-si

Korea, Republic of

Offenbach / Main

Germany

Id

Name

City

Country

13360

Arnhem

Netherlands

13348

Reichenwalde b. Berlin

Germany

13371

Kista

Sweden

13365

Singapore

Singapore

13359

Gyeonggi-do

Korea, Republic of

13641

Paris Cedex 15

France

13361

Lysaker

Norway

13334

BRUSSELS 1070

Belgium

13342

Helsinki

Finland

13354

Yokohama

Japan

13345

Nürnberg

Germany

13346

München

Germany

13340

Ballerup

Denmark

13344

Offenbach / Main

Germany

Id

Name

City

Country

13347

Hartmannsdorf

Germany