IEC 60601-1-9 Accredited Testing Labs Worldwide

11 accredited laboratories in 5 countries hold IEC 60601-1-9 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation.

Total labs

Countries

Available in 5 Countries

China

5 labs

United States

3 labs

Germany

1 lab

Finland

1 lab

Taiwan

1 lab

Top matrices for IEC 60601-1-9

Medical equipment, electrical safety and EMC

1 lab

Water

1 lab

Sample labs

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

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:

Eurofins Electrical Testing Service (Shanghai) Co.,

Shanghai, CN

IEC 60601-1-9; EN 60601-1-9; CAN/CSA-C22.2 NO. 60601-1-9 Medical Electrical Equipment –Part 1-11: General Requirements for Basic Safety and Essential Performance – Collateral Standard: Requirements for Medical Electrical Equipment a

Shenzhen CTL Testing Technology Co.,

Shenzhen, CN

IEC 60601-1-9; EN 60601-1-9 Medical electrical equipment - Part 1-12: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical system

SGS Taiwan

Taoyuan City, TW

IEC 60601-1-9; EN 60601-1-9; CAN/CSA C22.2 No. 60601-1-9 Home healthcare environment IEC 60601-1-11; EN 60601-1-11; ANSI/AAMI HA60601-1-11; CAN/CSA-C22.2 No. 60601-1-11 Emergency medical services environment IEC 60601-1-12; E

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

Shenzhen, Guangdong, CN

Test Technology: Test Method(s)2: Medical Equipment (continued) IEC 60601-2-40; EN 60601-2-40; CAN/CSA-C22.2 No. 60601-2-40;

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

Guangzhou, CN

IEC 60601-1-9; EN 60601-1-9; CAN/CSA C22.2 No. 60601-1-9

TUV Rheinland (Shanghai) Co.,

Shanghai, CN

IEC 60601-1-9; EN 60601-1-9; DIN EN 60601-1-9; VDE 0750-1-9; IEC 60601-1-9 Edition 1.2 2020-07 CONSOLIDATED VERSION Medical electrical equipment – Part 1-10: General requirements for basic safety and essential performance – Colla

Intertek Testing Services NA

Kentwood, MI, US

IEC 60601-1-9; IEC 60601-1-10; IEC 60601-1-10 Edition 1.2 2020-07 CONSOLIDATED VERSION; IEC 60601-1-11; IEC 60601-1-11:2015+AMD1:2020; IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED VERSION; ANSI AAMI HA60601-1-11:2015; ANSI A

Bay Area Compliance

Sunnyvale, CA, US

IEC 60601-1-9 (2007) IEC 60601-1-12 (2014); IEC 60601-2-37 (2015); IEC TR 60601-4-2 (2016); CAN/CSA C22.2 No. 60601-1 (2008); ANSI AAMI ES60601-1 (2005/(R)2012) and A1:2012, C1:2009/(R)2012 and A2:2010/(R) 2012 (Consolidated Text) [Inc

SGS Fimko

Helsinki, FI

IEC 60601-1-9 Medical electrical equipment - Part 2-25: Particular requirements for the basic safety and essential performance of electrocardiographs IEC 60601-2-25; ANSI/AAMI/IEC 60601-2-25