IEC 60601-2-22 Accredited Testing Labs Worldwide

41 accredited laboratories in 10 countries hold IEC 60601-2-22 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle, Italian Accreditation Body.

Total labs

Countries

Top matrix

Medical equipment, electrical safety and EMC

3 labs

Available in 10 Countries

China

14 labs

Japan

2 labs

Canada

2 labs

Taiwan

2 labs

Netherlands

1 lab

United Kingdom

1 lab

South Korea

1 lab

Top matrices for IEC 60601-2-22

Medical equipment, electrical safety and EMC

3 labs

Electrical equipment

1 lab

Sample labs

SGS-CSTC Standard Technical Services Co., Ltd. Wuhan Branch

Wuhan, CN

IEC 60601-2-22; IEC 60601-2-28 2; IEC 60601-2-36; IEC 60601-2-37; IEC 60601-2-43 2; IEC 60601-2-44 2; IEC 60601-2-45 2; IEC 60601-2-54 2; IEC 60601-2-57; IEC 80601-2-60; IEC 60601-2-63 2; IEC 60601-2-65 2; EN 60601-1; EN 60601

TUV SUD Certification and Testing (China) Co.,

Wuxi, CN

IEC 60601-2-22 Edition 4.0 2019-11; IEC 60601-2-25 Edition 2.0 2011-10; ANSI AAMI IEC 60601-2-25:2011/(R)2016; IEC 60601-2-27 Edition 3.0 2011-03; ANSI AAMI IEC 60601-2-27:2011(R)2016; IEC 60601-2-28 Edition 3.0 2017-06; IEC 60601-2-3

TUV SUD Japan Ltd. Yonezawa Testing Center (EMC Lab)

Yamagata, JP

IEC 60601-2-22; EN IEC 60601-2-22; JIS T 0601-2-22 (clause 202 only); IEC 60601-2-24; EN 60601-2-24; JIS T 0601-2-24 (clause 202 only); IEC 60601-2-25; EN 60601-2-25; JIS T 0601-2-25; ANSI AAMI IEC 60601-2-25 (clause 202 only); IEC

TÜV SÜD Certification and Testing (China) Co., Ltd. Guangzhou Branch

China, DE

IEC 60601-2-22; IEC 60601-2-22:2007; IEC 60601-2-22 Edition 3.1 2012-10; IEC 60601-2-22 Edition 4.0 2019-11; CSA C22.2 No. 60601-2-22; EN IEC 60601-2-22 IEC 60601-2-37; IEC 60601-2-37 Edition 2.1 2015; IEC 60601-2-37 Edition 3.0 2

Lasermet

Dorset, GB

IEC 60601-2-22:2013 BS EN 60825-12:2004 BS EN 60825-1:2001 BS EN 60825-1 2007 BS EN 60825-1:2014 BS EN 60825-1:2014 +A11:2021 IEC 60825-1:2014 Lab Lab Lab Lab Lab Lab Lab

Element Materials Technology Irvine

Irvine, CA, US

IEC 60601-2-22; EN 60601-2-22; CAN/CSA-C22.2 No. 60601-2-22 excluding 201.12.1.101, 201.12.4.2, 201.13.1.101, 201.13.2; IEC 60601-2-24; EN 60601-2-24; IEC 60601-2-30; EN 606

TÜV Rheinland LGA Products

Nürnberg, DE

IEC 60601-2-22 : 2022-10 DIN EN 60601-2-25 : 2016-08 DIN EN 60601-2-26 : 2016-02 DAkkS Deutsche Akkreditierungsstelle DIN EN 60601-2-20 : 2010-060 - Medizinische elektrische Geräte - Teil 2-20: Besondere Festlegungen für die Sicherheit eins

TÜV Rheinland Japan Ltd. Yokohama Laboratories Global Technology Assessment Center

Japan, DE

Department Standard / in house procedure / Version Title of standard or in house procedure (deviaBons /reducBons modiﬁcaBons of standard) LocaBon/ reducBons Product Safety IEC 60601 -2-10:2012 + A1:2016 IEC 60601-2- 10:201

SGS-CSTC Standards Technical Services (Shanghai) Co.,

Xinqiao, Songjiang, Shanghai, CN

IEC 60601-2-22 (Excluding Cl 201.10, 201.10.4, 201.12.1, 201.12.4, 201.13.1, 201.13.2, 201.17); IEC 60601-2-23 (Excluding Cl 201.17, 202); IEC 60601-2-24 (Excluding Cl 201.11.6.3, 201.11.6.5, 201.17, 202); IEC 60601-2-25 (Excludi

VDE Prüf- und Zertifizierungsinstitut

Offenbach am Main, DE

IEC 60601-2-22 − equipment with non-laser light source for use in therapy, diagnosis, monitoring and for cosmetic/aesthetic purposes DIN EN 60601-2-57 IEC 60601-2-57 − infant phototherapy equipment Compliance tests for basi

TUV SUD Canada

Gormley, ON, CA

IEC 60601-2-22; IEC 60601-2-22 Edition 3.1 2012-10 1; IEC/EN 61326-3-1; EN 16361; ISO 13849-1; ISO 13849-2; EN ISO 13850; EN ISO 13857; EN ISO 14119; EN ISO 13855; EN ISO 14120; EN ISO 4414; EN ISO 12100; IEC/EN 60204-1; EN 415-3;

CSA Group Bayern

Plattling, DE

IEC 60601-2-22 : 2022-10 Medizinische elektr ische Geräte - Teil 2-22: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale für chirurgische, kosmetische, therapeutische und diagnostische Lasergerät

Intertek Testing Services NA

Duluth, GA, US

IEC 60601-2-22 Edition 3.1 2012-10 12-268 IEC 60601-2-22 Edition 4.0 2019-11 12-356 IEC 60601-2-23 Edition 3.0 2011-02 1-87 IEC 60601-2-25 Edition 2.0 2011-10 3-105 ANSI AAMI IEC 60601-2-25:2011/(R)2016 3-105 IEC 60601-2-27 Edition 3.0

Eurofins Electrical Testing Service (Shenzhen) Co.,

Shenzhen City, Guangdong, CN

Test Technology: Test Method(s) 2,3,4: Part 1-11: General requirements for basic safety and essential performance -- Collateral Standard: Requirements for medical electrical equipment and medical electrical equipment and medical ele

MEGALAB Group

Aurora, ON, CA

IEC 60601-2-22 Edition 3.1 2012-10 12-268 2 These methods have been assessed by A2LA according to A2LA’s FDA ASCA Program requirements. Accreditation by A2LA does not imply FDA ASCA-Accreditation. All ASCA-accreditation decisions for

Shenzhen Huatongwei International Inspection Co.,

Shenzhen, CN

IEC 60601-2-22 Edition 3.1 2012-10 12-268 IEC 60601-2-25 Edition 2.0 2011-10 3-105

MedTech Testing Solution Co.,

New Taipei City, TW

IEC 60601-2-22; EN IEC 60601-2-22; BS EN IEC 60601-2-22; CAN/CSA C22.2 No. 60601-2-22; AS IEC 60601.2.22

Eurofins Electrical Testing Service (Shanghai) Co.,

Shanghai, CN

IEC 60601-2-22; EN IEC 60601-2-22; CSA-C22.2 NO. 60601-2-22 Medical Electrical Equipment – Part 2-24: Particular Requirements for the Basic Safety and Essential Performance of Infusion Pumps and Controllers IEC 60601-2-24; EN 60601

Shenzhen CTL Testing Technology Co.,

Shenzhen, CN

IEC 60601-2-22; EN IEC 60601-2-22 Medical electrical equipment - Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment IEC 60601-2-40; EN IEC 60601-2-40

Element Materials Technology Fremont Newark

Fremont, CA, US

Test: Test Method(s) 1: Generic and Product Family Standards (cont.) IEC 62236-4; EN 50155; EN 55013; KN 13; EN 55020 (only for audio/video equipment without tuner); KN 20 (only for audio/video equipment without tuner); EN 50

SGS Taiwan

Taoyuan City, TW

IEC 60601-2-22; EN IEC 60601-2-22; CAN/CSA-C22.2 No. 60601-2-22 Electrocardiographs IEC 60601-2-25; EN 60601-2-25; ANSI/AAMI 60601-2- 25; CAN/CSA C22.2 No. 60601-2-25; JIS T 0601-2-25 Electrocardiographic monitoring equipment

TÜV SÜD Product Service

Frankfurt/Main, DE

IEC 60601-2-22 : 2022-10 Medizinische elektrische Geräte - Teil 2-22: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale für chirurgische, kosmetische, therapeutische und diagnostische Lasergeräte

Intertek Deutschland

Kaufbeuren, DE

IEC 60601-2-22:2019) ; Deutsche Fassung EN IEC 60601-2-22:2020 DIN EN 60601-2-26 : 2004-01 ⊗ Medizinische elektrische Geräte - Teil 2-26: Beson dere Festlegungen für die Sicherheit von Elektroenzephal ographen (IEC 60601-2-26:2002); De

SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch

Shenzhen, Guangdong, CN

IEC 60601-2-22; EN IEC 60601-2-22; CAN/CSA-C22.2 No. 60601-2-22; IEC 60601-2-24; EN 60601-2-24; CAN/CSA-C22.2 No. 60601-2-24; IEC 60601-2-25; EN 60601-2-25; ANSI/AAMI 60601-2-25; CAN/CSA C22.2 No. 60601-2-25; IEC 80601-2-26

DEKRA Testing and Certification (Shanghai) Ltd., Guangzhou Branch

Guangzhou, CN

IEC 60601-2-22; EN IEC 60601-2-22; CAN/CSA-C22.2 No. 60601-2-22 Safety of laser products - Part 1: Equipment classification and requirements IEC 60825-1; EN 60825-1; CSA E60825-1 Medical electrical equipment – Part 2-24: Particul

TUV Rheinland (Shanghai) Co.,

Shanghai, CN

IEC 60601-2-22; EN 60601-2-22; DIN EN 60601-2-22; VDE 0750-2-22; IEC 60601-2-22 Edition 3.1 2012-10; IEC 60601-2-22 Edition 4.0 2019-11 Medical electrical equipment - Part 2-24: Particular requirements for the basic safety and ess

Intertek Testing Services NA

Kentwood, MI, US

IEC 60601-2-22; IEC 60601-2-22 Edition 3.1 2012-10; IEC 60601-2-22 Edition 4.0 2019-11; IEC 60601-2-25; IEC 60601-2-25 Edition 2.0 2011-10; IEC 60601-2-27; IEC 60601-2-27 Edition 3.0 2011-03; IEC 60601-2-36; IEC 60601-2-36 Edition 2.0

F2 Labs

Middlefield, OH, US

IEC 60601-2-22 Edition 3.1 2012-10 (Section(s) 201.17/202) 1; IEC 60601-2-22 Edition 4.0 2019-11; IEC 60601-2-23 Edition 3.0 2011-02 (Section(s) 201.17/202) 1; IEC 60601-2-25 Edition 2.0 2011-10 1; ANSI AAMI IEC 60601-2-25:2011/(R)201

TUV Rheinland of North America

Pleasanton, CA, US

IEC 60601-2-22 Edition 3.1 2012-10 12-268 IEC 60601-2-22 Edition 4.0 2019-11 12-356

SGS Korea Co., Ltd. (Gunpo Laboratory)

Gunpo-si, KR

Test Technology: Test Method(s) 1, 4: Product Safety Measurement Equipment2, 3 IEC/EN/KS C IEC/UL 61010-1; CAN/CSA C22.2 No. 61010-1; IEC/EN 61010-2-010; IEC/EN 61010-2-020; IEC/EN 61010-2-040; IEC/EN 61010-2-051; IEC/EN 61010-2-08

DEKRA Testing and Certification (Suzhou) Co.,

Suzhou, Jiangsu Province, CN

IEC 60601-2-22; CSA C22.2 No. 60601-2-22 Medical electrical equipment – Part 2-28: Particular requirements for the basic safety and essential performance of X-ray tube assemblies for medical diagnosis IEC/ EN IEC 60601-2-28; CSA

TUV Rheinland (China)

Beijing, CN

IEC 60601-2-22 Edition 4.0 2019-11 (excluding clauses listed in the “Exclusion” table above) 12-356 IEC 60601-2-37 Edition 2.1 2015 (excluding clauses listed in the “Exclusion” table above) 12-293 IEC 60601-2-52 Edition 1.1 2015-0

SLG Prüf- und Zertifizierungs

Hartmannsdorf, DE

IEC 60601-2-22:2019); German version EN IEC 60601-2- 22:2020 DIN EN 60601-2-22 : 2015-08 ⊗ - Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic

Nemko S.p.A. a socio unico

Biassono, IT

IEC 60601-2-22:2021, EN IEC 60601-2-22:2020, IEC 60601-2-22:2019 _ Par 04 - Prescrizioni generali/General requirements, Par 05 - Prescrizioni generali per le prove sugli apparecchi EM/General requirements for testing ME Equipment, Par 06

TÜV Rheinland (Shanghai) Co.,

China, DE

IEC 60601-2-22:2007 + A1:2012); German version EN 60601-2- 22:2013 Medical Equipment IEC 60601 -2-24:2012 Medical electrical equipment - Part 2 -24: Particular requirements for the basic safety and essential performance of infu

White Lab S.r.l. - Test'ing

Falconara Marittima, IT

TUV Rheinland (Shenzhen) Co.,

Shenzhen, CN

IEC 60601-2-22 Edition 4.0 2019-11; IEC 60601-2-22 Edition 3.1 2012-10 12-356 12-268 IEC 60601-2-25 Edition 2.0 2011-10; ANSI/AAMI IEC 60601-2-25:2011/(R)2016 3-105 IEC 60601-2-27 Edition 3.0 2011-03; ANSI/AAMI IEC 60601-2-27:2011(R

TUV SUD Japan

Tokyo, JP

IEC 60601-2-22:1995; EN 60601-2-22:1996; IEC 60601-2-22:2007; IEC 60601-2-22:2007 + A1:2012; IEC 60601-2-22:2019; CAN/CSA-C22.2 No. 60601-2-22:23; IEC 60601-2-25:2011 (Excluding Section 202); EN 60601-2-25:2015 (Excluding Section 2

Kiwa Nederland

RIJSWIJK ZH, NL

Normative document: EN ISO/IEC 17025:2017 Registration number: L 015 of Kiwa Nederland B.V. Kiwa FSS Testing This annex is valid from: 29-01-2026 to 01-09-2028 Replaces annex dated: 28-01-2026 Dutch Accreditation Council RvA

TUV Rheinland Italia

Pogliano Milanese, IT

TUV Rheinland Italia S.r.l. Via Mattei 3 20005 Pogliano Milanese MI Allegato al certificato di accreditamento n. 00321 rev. 5 del 25/06/2025 UNI CEI EN ISO/IEC 17025:2018 Revisione: 72 Sede A Data: 29/09/2025 pag. 9 di 64 Appar

TUV SUD America

San Diego, CA, US