IEC 60601-2-43 Accredited Testing Labs Worldwide

20 accredited laboratories in 6 countries hold IEC 60601-2-43 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.

Total labs

Countries

Available in 6 Countries

Germany

8 labs

China

6 labs

United States

3 labs

Canada

1 lab

Japan

1 lab

South Korea

1 lab

Top matrices for IEC 60601-2-43

Medical equipment, electrical safety and EMC

2 labs

Sample labs

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

Wuhan, CN

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 60601-1-3 2;

UL International Germany

Neu-Isenburg, DE

IEC 60601-2-43:2010 + A1:2017 + A2:2019); Deutsche Fassung EN 60601-2-43:2010 + AC:2014 + A1:2018 + A2:2020 DIN EN IEC 60601-2-46 : 2020-04 Medizinische elektr ische Geräte - Teil 2-46: Besondere Festlegungen für die Sicherheit einschli

TUV SUD Certification and Testing (China) Co.,

Wuxi, CN

IEC 60601-2-43 Edition 2.2 2019-10 CONSOLIDATED VERSION; IEC 60601-2-43 Edition 3.0 2022-12; IEC 60601-2-44 Edition 3.2: 2016; IEC 60601-2-47 Edition 2.0 2012-02; ANSI AAMI IEC 60601-2-47:2012/(R)2016; IEC 60601-2-50 Edition 3.0 2020-0

Intertek Japan K.K.

Tokyo, JP

IEC 60601-2-43 (Ed 2, Ed 2.1); IEC 60601-2-43 Edition 3.0 2022-12; IEC 60601-2-44; IEC 60601-2-44 Edition 3.2: 2016; IEC 60601-2-46; IEC 60601-2-52; IEC 60601-2-52 Edition 1.1 2015-03 CONSOLIDATED VERSION; IEC 60601-2-52 Edition 1

TÜV Rheinland LGA Products

Nürnberg, DE

IEC 60601-2-43 : 2024-02 DIN EN 60601-2-44 : 2017-03 DAkkS Deutsche Akkreditierungsstelle Medizinische elektrische Geräte - Teil 2-36: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Geräten z

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 -2-37:2007 + A1:2015 EN 60601-2-37/A1:20

VDE Prüf- und Zertifizierungsinstitut

Offenbach am Main, DE

IEC 60601-2-43 : 2020-12 Medizinische elektrische Geräte - Teil 2 -43: Beso ndere Festlegungen für die Sicherheit und wesentlichen Leistungsmerkmale von Röntgeneinrichtungen für interventionelle Verfahren (IEC 60601 -2-43:2010 + A1:2017

TUV SUD Canada

Gormley, ON, CA

IEC 60601-2-43 Edition 2.2 2019-10 CONSOLIDATED VERSION; IEC 60601-2-43 Edition 3.0 2022-12; IEC 60601-2-44 Edition 3.2: 2016; IEC 60601-2-45 Edition 3.1 2015; IEC 60601-2-47 Edition 2.0 2012-02; ANSI AAMI IEC 60601-2-47:2012/(R)2016;

CSA Group Bayern

Plattling, DE

IEC 60601-2-43:2010 + A1:2017 + A2:2019); Deutsche Fassung EN 60601-2-43:2010 + AC:2014 + A1:2018 + A2:2020 VDE 0750-2-43:2020-12 DIN EN 60601-2-43 : 2011-03 ⊗ - Medizinische elektrische Geräte - Teil 2-43: Besondere Festlegungen für

Intertek Testing Services NA

Duluth, GA, US

IEC 60601-2-43 Edition 2.2 2019-10 CONSOLIDATED VERSION 12-329 IEC 60601-2-43 Edition 3.0 2022-12 12-351 IEC 60601-2-44 Edition 3.2: 2016 12-302

TÜV SÜD Product Service

Frankfurt/Main, DE

IEC 60601-2-43:2010 + A1:2017 + A2:2019); Deutsche Fassung EN 60601-2-43:2010 + AC:2014 + A1:2018 + A2:2020 DIN EN 60601-2-43 : 2019-040 - Medizinische elektrische Geräte - Teil 2-43: Besondere Fest-legungen für die Sicherheit und we

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

Shenzhen, Guangdong, CN

IEC 60601-2-43; EN IEC 60601-2-43; IEC 60601-2-35; EN IEC 60601-2-35; EN 1789; EN 13718-1; ANSI/AAMI MP80601-2-49; CSA C22.2 No. 80601-2-56; CSA C22.2 No. 80601-2-90; CSA C22.2 No. 60601-2-50; CAN/CSA-C22.2 No. 60601-2-43;

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

Guangzhou, CN

IEC 60601-2-43; EN 60601-2-43; CAN/CSA C22.2 No. 60601-2-43 Medical electrical equipment – Part 2-44: Particular requirements for basic safety and essential performance of X-ray equipment for computed tomography IEC 60601-2-44; EN

TUV Rheinland (Shanghai) Co.,

Shanghai, CN

IEC 60601-2-43; EN 60601-2-43; DIN EN 60601-2-43; VDE 0750-2-43; IEC 60601-2-43 Edition 2.2 2019-10 CONSOLIDATED VERSION; IEC 60601-2-43 Edition 3.0 2022-12 Medical electrical equipment − Part 2-44: Particular requirements for

F2 Labs

Middlefield, OH, US

IEC 60601-2-43 - Ed. 2.0 2010-03 (Section(s) 201.17/202) 1; IEC 60601-2-43 Edition 2.1 2017-05 CONSOLIDATED VERSION (Section(s) 201.17/202) 1; IEC 60601-2-43 Edition 3.0 2022-12(Section(s) 201.17/202); IEC 60601-2-44 Edition 3.2: 2016

TUV Rheinland of North America

Pleasanton, CA, US

IEC 60601-2-43 (X-ray Equipment for Interventional Procedures); EN/IEC 60601-2-44 (X-ray Equipment for Computed Tomography); EN/IEC 60601-2-45 (Mammographic X-ray Equipment and Mammographic Stereotactic Devices); EN/IEC 60601-2-46 (O

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

TUV Rheinland (China)

Beijing, CN

IEC 60601-2-43 Edition 2.2 2019-10 CONSOLIDATED VERSION (excluding clauses listed in the “Exclusion” table above) 12-329 IEC 60601-2-44 Edition 3.2: 2016 (excluding clauses listed in the “Exclusion” table above) 12-302 IEC 60601-2-5

SLG Prüf- und Zertifizierungs

Hartmannsdorf, DE

IEC 60601-2-43 Safety checks Non-ionizing radiation imaging devices Checking compliance with general and specific requirements - Ultrasound devices for diagnosis and monitoring DIN EN 60601-2-37 IEC 60601-2-37 Monitoring

TÜV Rheinland (Shanghai) Co.,

China, DE

Department Standard / in house procedure / Version Title of standard or in-house procedure (deviations / modifications of standard) Test area / reductions Medical Equipment # DIN EN 60601 -2-37:2016 VDE 0750-2-37:2016 Medica