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Registers collected 2026-08-04 to 2026-08-05.See collection dates

IEC 60601-2-16 Accredited Testing Labs Worldwide

17 accredited laboratories in 5 countries hold IEC 60601-2-16 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.

Total labs
17
Countries
5

Available in 5 Countries

China
6 labs
Germany
6 labs
United States
5 labs
Canada
1 lab
Japan
1 lab

Top matrices for IEC 60601-2-16

Medical equipment, electrical safety and EMC
2 labs

Sample labs

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

IEC 60601-2-16; IEC 60601-2-16 Edition 5.0 2018-4; IEC 60601-2-16:2025; ANSI AAMI IEC 60601-2-16; ANSI AAMI IEC 60601-2-16:2018; CSA C22.2 No. 60601-2-16; EN IEC 60601-2-16 IEC 60601-2-10; IEC 60601-2-10 Edition 2.1 2016-04; IEC

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

IEC 60601-2-16; EN IEC 60601-2-16; ANSI/AAMI/IEC 60601-2-16; CSA C22.2 NO. 60601-2-16; IEC 60601-2-24; EN 60601-2-24; CSA C22.2 NO. 60601-2-24 Defibrillators: IEC 60601-2-4; EN 60601-2-4; CSA-C22.2 NO. 60601-2-4 Endoscope Equipmen

TÜV Technische Überwachung Hessen GmbH EMV-Labor
Kassel, DE

IEC 60601-2-16 DIN EN 60601-2-24 IEC 60601-2-24 DIN EN IEC 60601-2-39 - Hämodialyse-, Hämodiafiltrations- und Hämofiltrationsgeräten - Infusionspumpen und - steuergeräte - Peritoneal-Dialyse-Geräte Beatmungs-, Sauerstof

TÜV Rheinland Japan Ltd. Yokohama Laboratories Global Technology Assessment Center
Japan, DE

IEC 60601-2-16 VDE 0750-2-16:2020-05 Medical electrical equipment - Part 2 -16: ParDcular requirements for basic safety and essenDal performance of haemodialysis, haemodiafiltraDon and haemofiltraDon equipment. A Product Safety IEC

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

IEC 60601-2-16 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-19 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-20 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-21 (Cl 201.10.6, 201.17, 202); ANSI/AAMI/IEC 60601-2-25 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-

TUV SUD Canada
Gormley, ON, CA

IEC 60601-2-16 Edition 5.0 2018-4; ANSI AAMI IEC 60601-2-16:2018; IEC 60601-2-18: Edition 3.0 2009-08; IEC 60601-2-19 Edition 3.0 2020-09; IEC 60601-2-21 Edition 3.0 2020-09; IEC 60601-2-22 Edition 3.1 2012-10; IEC 60601-2-22 Edition

UL LLC
Novi, MI, US

IEC 60601-2-16 Edition 5.0 2018-4 (clause 202 only) 9-121 IEC 60601-2-18: Edition 3.0 2009-08 (clause 202 only) 9-114 IEC 60601-2-19 Edition 3.0 2020-09 (clause 202 only) 6-461 IEC 60601-2-20 Edition 3.0 2020-09 (clause 202 only) 6-462

TÜV SÜD Product Service
Frankfurt/Main, DE

IEC 60601-2-16 : 2020-05 Medizinische elektrische Geräte - Teil 2-16: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hämodialyse-, Hämodiafiltrations- und Hämofiltrationsgeräten (IEC 60601

TUV Rheinland (Shanghai) Co.,
Shanghai, CN

IEC 60601-2-16; EN 60601-2-16; DIN EN 60601-2-16; VDE 0750-2-16; IEC 60601-2-16 Edition 5.0 2018-4; ANSI AAMI IEC 60601-2-16:2018 Medical electrical equipment – Part 2-18: Particular requirements for the safety of endoscopic equipm

Intertek Testing Services NA
Kentwood, MI, US

IEC 60601-2-16; IEC 60601-2-16 Edition 5.0 2018-4; IEC 60601-2-18; IEC 60601-2-18 Edition 3.0 2009-08; 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

F2 Labs
Middlefield, OH, US

IEC 60601-2-16:2018 (Section(s) 201.17/202) 1; IEC 60601-2-18: Edition 3.0 2009-08 (Section(s) 201.17/202) 1; ANSI AAMI IEC 60601-2-19 Edition 2.1 2016-04; ANSI AAMI IEC 60601-2-19 Edition 3.0 2020-09; ANSI AAMI IEC 60601-2-2:2017 (Se

TUV Rheinland of North America
Pleasanton, CA, US

IEC 60601-2-16 Edition 5.0 2018-4 9-121 ANSI AAMI IEC 60601-2-16:2018 9-121 IEC 60601-2-17 Edition 3.0 2013-11 12-272 IEC 60601-2-18 Edition 3.0 2009-08 9-114 ANSI AAMI IEC 60601-2-19:2009/(R)2014 & A1:2016 6-461 IEC 60601-2-20 Editi

Centre Testing International Group Co.,
Shenzhen, Guangdong, CN

IEC 60601-2-16 Edition 5.0 2018-4 9-121 IEC 60601-2-18 Edition 3.0 2009-08 9-114 IEC 60601-2-19 Edition 3.0 2020-09 6-461 IEC 60601-2-20 Edition 3.0 2020-09 6-462 IEC 60601-2-22 Edition 3.1 2012-10 12-268 IEC 60601-2-22 Edition 4.0 201

Medical Equipment Compliance Associates, LLC.
Oak Creek, WI, US

IEC 60601-2-16; Endoscopic Equipment IEC 60601-2-18;

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 -2-7:2000 VDE 0750-2-7:2000 Medical el

TUV Rheinland (Shenzhen) Co.,
Shenzhen, CN

IEC 60601-2-16 Edition 5.0 2018-4; ANSI/AAMI IEC 60601-2-16:2018 9-121 IEC 60601-2-18 Edition 3.0 2009-08 9-114 IEC 60601-2-19 Edition 3.0 2020-09 6-461 IEC 60601-2-2 Edition 6.0 2017-03; ANSI/AAMI IEC 60601-2-2:2017 6-389 IEC 60601

TUV SUD Japan
Tokyo, JP

IEC 60601-2-16:1998 (Excluding Section 19.4); EN 60601-2-16:1998 (Excluding Section 19.4); JIS T 0601-2-16:2008 (Excluding Section 19.4); IEC 60601-2-16:2008 (Excluding Section 201.12.4.4.101); IEC 60601-2-16:2012 (Excluding Section 201