IEC 60601-1-8 Accredited Testing Labs Worldwide

43 accredited laboratories in 11 countries hold IEC 60601-1-8 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle. In the register, IEC 60601-1-8 scope entries most often cover Combustible Gasses, Leakage Radiation in Medical equipment, electrical safety and EMC, Medical devices.

Total labs

Countries

Top matrix

Medical equipment, electrical safety and EMC

4 labs

Available in 11 Countries

China

14 labs

United Kingdom

2 labs

Canada

2 labs

Finland

1 lab

Japan

1 lab

South Korea

1 lab

Netherlands

1 lab

Taiwan

1 lab

France

1 lab

Top matrices for IEC 60601-1-8

Medical equipment, electrical safety and EMC

4 labs

Medical devices

1 lab

Top analytes for IEC 60601-1-8

Combustible Gasses (1)
Leakage Radiation (1)

Sample labs

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

Wuhan, CN

IEC 60601-1-8; IEC TR 62366-2; IEC 60601-1-11; IEC 60601-2-2; IEC 60601-2-10; IEC 60601-2-18; 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

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

China, DE

IEC 60601-1-8; IEC 60601-1-8:2006; IEC 60601-1-8 Edition 2.1 2012-11; IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-8; ANSI AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021]; CSA C22.2 No. 606

QPS Evaluation Services

Toronto, ON, CA

IEC 60601-1-8; IEC 60601-2-10; IEC 60601-2-18; IEC 60601-2-2; IEC 60601-2-23; IEC 60601-2-25; IEC 60601-2-26; IEC 60601-2-27; IEC 60601-2-30; IEC 60601-2-32; IEC 60601-2-33; IEC 60601-2-34; IEC 60601-2-36; IEC 60601-2-4; IEC 6

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

Guangzhou, Guangdong, CN

IEC 60601-1-8; EN 60601-1-8; ANSI/AAMI/IEC 60601-1-8; CAN/CSA-C22.2 No. 60601-1-8; IEC 60601-1-11; EN 60601-1-11; ANSI/AAMI HA60601-1-11; CAN/CSA-C22.2 No. 60601-1-11; IEC 60601-1-12; EN 60601-1-12; ANSI/AAMI/IEC 60601-1-12; CAN/CSA-

TÜV Rheinland LGA Products

Nürnberg, DE

IEC 60601-1-8:2006 + A1:2012 + A2:2020); Deutsche Fassung EN 60601-1-8:2007 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2017 + A2:2021 DIN EN 60601-1-8 : 2014-04 - Medizinische elektrische Geräte - Teil 1-8: Allgemeine Festlegungen für di

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 EN 60601 -1- 6:2010/A1:2015 EN 60601-1- 6:2010/A2:2021 DIN EN 60

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

Xinqiao, Songjiang, Shanghai, CN

IEC 60601-1-8; IEC 60601-1-10; IEC 60601-1-11 (Excluding Cl 4.2, 8.3, 10.1, 12); IEC 60601-1-12 (Excluding Cl 6.2, 8.1, 10.1, 12); IEC 60601-2-16 (Excluding Cl 201.17); IEC 60601-2-2 (Excluding Cl 201.17, 202); IEC 60601-2-3 (Excludi

VDE Prüf- und Zertifizierungsinstitut

Offenbach am Main, DE

This document is a translation. The definitive version is the original German annex to the accreditation certificate. Geräten und in medizinischen elektrischen Systemen (IEC 60601-1- 8:2006 + A1:2012); Deutsche Fassung EN 60601 -1-8:2007

TUV SUD Canada

Gormley, ON, CA

IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021]; IEC 60601-1-10 Edition 1.2 2020-07 CONSOLIDATED VERSION; IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED VERSION;

CSA Group Bayern

Plattling, DE

IEC 60601-1-8:2003 + A1:2006); Deutsche Fassung EN 60601-1- 8:2004 + A1:2006 DIN EN 60601-1-8 : 2004-09 ⊗ - Medizinische elektrische Geräte - Teil 1-8: Allgemeine Festlegungen für die Sicherheit - Ergänzungsnorm: Alarmsysteme - Allgeme

Intertek Testing Services NA

Duluth, GA, US

Tests: Standard(s) 2: Laboratory / Process Control / Test Equipment Products (excluding UV Radiation, Flammable Liquids, Cathode ray tubes test) (continued) UL 61010-2-040:2021, Ed. 3; UL 61010-2-051:2015, Ed. 3; UL 61010-2-051:

Device Conformity and Testing

Devens, MA, US

IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION 5-131 IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED VERSION 19-38 IEC 60601-2-2 Edition 6.0 2017-03 6-389 IEC 60601-2-64:2014-09 12-318 IEC 60601-2-68 Edition 1.0 2014-09 12-319

Eurofins Electrical Testing Service (Shenzhen) Co.,

Shenzhen City, Guangdong, CN

IEC 60601-1-8; CAN/CSA-C22.2 NO. 60601-1-8A

Shenzhen Huatongwei International Inspection Co.,

Shenzhen, CN

IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION 5-131 IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED VERSION 19-38 IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION 19-39 IEC 60601-2-2 Edition 6.0 2017-03 6-389 IEC 60601-

MedTech Testing Solution Co.,

New Taipei City, TW

IEC 60601-1-8; EN 60601-1-8; BS EN 60601-1-8; CAN/CSA-C22.2 No. 60601-1-8; AS IEC 60601.1.8; JIS T 60601-1-8; ANSI AAMI IEC 60601-1-8 Medical electrical equipment and medical electrical systems used in the home healthcare env

Eurofins Electrical Testing Service (Shanghai) Co.,

Shanghai, CN

IEC 60601-1-8; EN 60601-1-8; ANSI/AAMI/IEC 60601-1-8; CAN/CSA-C22.2 NO. 60601-1-8 Medical Electrical Equipment - Part 1-9: General Requirements for Basic Safety and Essential Performance - Collateral Standard: Requirements for Envi

Shenzhen CTL Testing Technology Co.,

Shenzhen, CN

IEC 60601-1-8; EN 60601-1-8; ANSI AAMI IEC 60601-1-8 Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and

TÜV SÜD Product Service

Frankfurt/Main, DE

IEC 60601-1-8:2006 + A1:2012 + A2:2020); Deutsche Fassung EN 60601-1-8:2007 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2017 + A2:2021 DIN EN 60601-1-8 : 2014-040 - Medizinische elektrische Geräte - Teil 1-8: Allgemeine Festlegungen f

Eurofins Product Service

Reichenwalde, DE

IEC 60601-1-8 : 2006-10 Medical electrical equipmen t - Part 1-8: General requirements for basic safety and essential performance - Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equ

LNE - LABORATOIRES DE TRAPPES

TRAPPES, FR

IEC 60601-1-8 Paragraphe 6.3.3.2

Intertek Deutschland

Kaufbeuren, DE

IEC 60601-1-8: 2006 + A1:2012 + A2:2020); Deutsche Fassung EN 60601-1-8:2 007 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2017 + A2:2021 VDE 0750-1-8:2021-12 DIN EN 60601-1-8 : 2014-04 ⊗ - Medizinische elektrische Geräte - Teil 1-8:

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

Shenzhen, Guangdong, CN

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

Guangzhou, CN

IEC 60601-1-8; EN 60601-1-8; ANSI/AAMI/IEC 60601-1-8; CAN/CSA-C22.2 No. 60601-1-8 Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance – Collateral standard: Requirements for envi

TUV Rheinland (Shanghai) Co.,

Shanghai, CN

IEC 60601-1-8; EN 60601-1-8; DIN EN 60601-1-8; VDE 0750-1-8; IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021] Medical electrical equipment –Part 1-9:

Intertek Testing Services NA

Kentwood, MI, US

IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021]; ANSI/AAMI HA60601-1-11:2015; ANSI/AAMI HA60601-1-11:2015 [Including AMD1: 2021] (The above standards exclude Clauses 10.1.2 Requirements for mechanical strength for

TUV Rheinland of North America

Pleasanton, CA, US

IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION 5-131 ANSI AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021] 5-131 IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED 19-38 HA60601-1-11:2015 [Including AMD1:2021] 19-47 ANSI

cetecom advanced

Saarbrücken, DE

IEC 60601-1-8:2006 + A1:2012 + A2:2020); Deutsche Fassung EN 60601-1-8:2007 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2017 + A2:2021 DIN EN 60601-1-8 : 2014-04 ⊗ - Medizinische elektrische Geräte - Teil 1-8: Allgemeine Festlegunge

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 60601-1-8; EN 60601-1-8; ANSI/AAMI/IEC 60601-1-8; CAN/CSA-C22.2 No. 60601-1-8 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance – Collateral standard: Requirements for medical

TÜV Rheinland Korea Ltd. Test Center, Safety of Electrical Appliances and Ergonomics

Republic Of, DE

The testing laboratory is permitted, without being required to inform and obtain prior approval from DAkkS, to use standards or equivalent testing methods listed here with different issue dates. The testing laboratory maintains a current

TUV Rheinland (China)

Beijing, CN

IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION (excluding clauses listed in the “Exclusion” table above) 5-131 IEC 60601-2-43 Edition 2.2 2019-10 CONSOLIDATED VERSION (excluding clauses listed in the “Exclusion” table above)

Element Materials Technology - Hull

Kingston upon Hull, GB

IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021]; CSA CAN/CSA-C22.2 No. 60601-1-8:08 - Medical electrical equipment - Part 1-8; IEC 60601-1-11 Edition 2.1 2020-07 C

SLG Prüf- und Zertifizierungs

Hartmannsdorf, DE

IEC 60601-1-8:2006 + A1:2012 + A2:2020); German version EN 60601-1-8:2007 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2017 + A2:2021 DIN EN 60601-1-8 : 2014-04 ⊗ - Medical electrical equipment - Part 1-8: General requirements for ba

Medical Equipment Compliance Associates, LLC.

Oak Creek, WI, US

IEC 60601-1-8; IEC 60601-1-8:2006 + A1:2012 + A2:20201; ANSI/AAMI/IEC 60601-1-8; ANSI/AAMI/IEC 60601-1- 8:2006 + A1:2012 + A2:20211; CAN/CSA C22 No. 60601-1-8; EN 60601-1-8; Requirements for Physiological Closed-Loop Controlle

Sigma Scientific Services

Sunrise, FL, US

IEC 60601-1-8:2006 and A1:2012 General methods of measuring the performance of ultrasonic pulsed-echo diagnostic equipment JIS T 1501: 2005 Ultrasonics –Characteristic of Fields IEC 61846 Edition 1998-04; IEC 63045 Edition 2020-05;

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 -1-8:2021 -12 VDE

SGS Fimko

Helsinki, FI

IEC 60601-1-8; ANSI/AAMI/IEC 60601-1-8 Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design IEC 60601-1-9

Kiwa Primara

Kaufbeuren, DE

IEC 60601-1-8 : 2012-11 Medical electrical equipmen t - Part 1-8: General requirements for basic safety and essential performance - Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equ

Intertek Testing & Certification

Essex, GB

IEC 60601-1-8:2006 +A1 EN 60601-1-8:2007 +A1 IP, S Medical electrical equipment Home healthcare Electrical safety Environmental conditioning IEC 60601-1-11:2015 EN 60601-1-11:2015 IEC 60601-1-11:2010 EN 60601-1-11:2010

TUV Rheinland (Shenzhen) Co.,

Shenzhen, CN

IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION; ANSI/AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021] 5-131 IEC 60601-2-10 Edition 2.1 2016-04 17-16 ISO 80601-2-13 Second edition 2022-04; ISO 80601-2-13 First edition

TUV SUD Japan

Tokyo, JP

IEC 60601-1-8:2003 + A1:2006; IEC 60601-1-8:2006; IEC 60601-1-8:2006 + A1:2012 + A2:2020; EN 60601-1-8:2007 + A1:2013 + A2: 2021; JIS T 60601-1-8:2012; IEC 60601-1-11:2010 (Excluding Sections 4.2, 10.1, 12); IEC 60601-1-11:2015 (

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 SUD America

San Diego, CA, US

IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION 5-131 ANSI AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021] 5-131 IEC 60601-1-10 Edition 1.2 2020-07 CONSOLIDATED VERSION 19-37 IEC 60601-1-11 Edition 2.1 2020-07 CONSOLI