IEC 60601-2-33 Accredited Testing Labs Worldwide

17 accredited laboratories in 5 countries hold IEC 60601-2-33 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.

Total labs

Countries

Available in 5 Countries

Germany

6 labs

China

4 labs

United States

4 labs

Canada

2 labs

Japan

1 lab

Top matrices for IEC 60601-2-33

Medical equipment, electrical safety and EMC

1 lab

Sample labs

TUV SUD Certification and Testing (China) Co.,

Wuxi, CN

IEC 60601-2-33 Edition 4.0 2022-08; IEC 60601-2-34 Edition 3.0 2011-05; IEC 60601-2-35 Edition 2.0 2020-09; IEC 60601-2-35 Edition 2.1 2023-12 CONSOLIDATED VERSION; IEC 60601-2-37 Edition 2.1 2015; IEC 60601-2-37 Edition 3.0 2024-07;

QPS Evaluation Services

Toronto, ON, CA

IEC 60601-2-33; IEC 60601-2-34; IEC 60601-2-36; IEC 60601-2-4; IEC 60601-2-40

Intertek Japan K.K.

Tokyo, JP

IEC 60601-2-33; IEC 60601-2-33 Ed. 3.2 b: 2015; IEC 60601-2-33 Edition 4.0 2022-08; IEC 60601-2-37 IEC 60601-2-37 Edition 2.1 2015; IEC 60601-2-38; IEC 60601-2-41; IEC 60601-2-43 (Ed 2, Ed 2.1); IEC 60601-2-43 Edition 3.0 2022-12;

TÜV Rheinland LGA Products

Nürnberg, DE

IEC 60601-2-33:2010 + COR1:2012 + A1:2013 + A2:2015 + COR2:2016); Deutsche Fassung EN 60601-2- 33:2010 + Cor.:2010 + A11:2011 + A1:2015 + A2:2015 + AC:2016 + Al2:2016 DIN EN 60601-2-33 : 2011-070 - Medizinische elektrische Geräte - Teil 2-3

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 -2-25:2011 EN 60601-2-25:2015 DIN IEC 6

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

Xinqiao, Songjiang, Shanghai, CN

IEC 60601-2-336 (Excluding Cl 201.17, 202); IEC 60601-2-34 (Excluding Cl 201.17, 202); IEC 60601-2-35 (Excluding Cl 201.17, 202); IEC 60601-2-36 (Excluding Cl 201.17, 202); IEC 60601-2-37 (Excluding Cl 201.11.6.5, 201.17, 202.6); IEC 6

TUV SUD Canada

Gormley, ON, CA

IEC 60601-2-33 Ed. 3.2 b:2015; IEC 60601-2-33 Edition 4.0 2022-08; IEC 60601-2-34 Edition 3.0 2011-05; IEC 60601-2-35 Edition 2.0 2020-09; IEC 60601-2-37 Edition 2.1 2015; IEC 60601-2-43 Edition 2.2 2019-10 CONSOLIDATED VERSION; IEC 6

CSA Group Bayern

Plattling, DE

IEC 60601-2-33 : 2022-08 Medical electrical equipme nt - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis CSA-C22.2 No. 60601-2-33:23 IEC 60601-2-33

Intertek Testing Services NA

Duluth, GA, US

IEC 60601-2-33 Ed. 3.2 b:2015 12-295 IEC 60601-2-33 Edition 4.0 2022-08 12-347 IEC 60601-2-34 Edition 3.0 2011-05 3-115 IEC 60601-2-35 Edition 2.0 2020-09 6-483 IEC 60601-2-37 Edition 2.1 2015 12-293 IEC 60601-2-43 Edition 2.2 2019-10

UL LLC

Novi, MI, US

IEC 60601-2-33 Ed. 3.2 b:2015 (clause 202 only) 12-295 IEC 60601-2-34 Edition 3.0 2011-05 (clause 202 only) 3-115 IEC 60601-2-36 Edition 2.0 2014-04 (clause 202 only) 9-119 IEC 60601-2-37 Edition 2.1 2015 (clauses 201.17, 202 only) 12-29

TÜV SÜD Product Service

Frankfurt/Main, DE

IEC 60601-2-33:2010 + Cor1:2012 + A1:2013 + A2:2015 + Cor2:2016); Deutsche Fassung EN 60601-2-33:2010 + Cor.:2010 + A11:2011 + A1:2015 + A2:2015 + AC:2016 + A12:2016 DIN EN 60601-2-33 : 2011-07⊗ - Medizinische elektrische Geräte - Tei

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

Shenzhen, Guangdong, CN

IEC 60601-2-33; EN 60601-2-33; CAN/CSA-C22.2 NO. 60601-2-33; IEC 60601-2-34; EN 60601-2-34; CAN/CSA C22.2 No. 60601-2-34; IEC 80601-2-35; EN 80601-2-35; ANSI/AAMI/ISO 80601-2-35; CAN/CSA-C22.2 NO. 80601-2-35; IEC 60601-2-37

TUV Rheinland (Shanghai) Co.,

Shanghai, CN

IEC 60601-2-33; EN 60601-2-33; DIN EN 60601-2-33; VDE 0750-2-33; IEC 60601-2-33 Ed. 3.2 b:2015; IEC 60601-2-33 Edition 4.0 2022-08 Medical electrical equipment − Part 2-37: Particular requirements for the basic safety and essentia

F2 Labs

Middlefield, OH, US

IEC 60601-2-33 Edition 4.0 2022-08 (Section(s) 201.17/202) 1; IEC 60601-2-34 Edition 3.0 2011-05 (Section(s) 201.17/202) 1; IEC 60601-2-36 Edition 2.0 2014-04 (Section(s) 201.17/202) 1; IEC 60601-2-37 Edition 2.1 2015 (Section(s) 201.1

TÜV SÜD Product Service GmbH PS-SL-EMC / PS-SL-ENV-STR

Straubing, DE

IEC 60601-2-33 : 2010-03 K DAkkS Deutsche Akkreditierungsstelle Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators + Corrigendum 1 : 2012-02 + Amendment 1 :

UL Verification Services

Fremont, CA, US

(A2LA Certificate No. 0751.05) Revised 03/02/2026 Page 3 of 10 Test Technology: Test Method(s) 1, 2: EMC Medical (continued) IEC/EN 60601-2-25 (cl. 202 only); IEC/EN 60601-2-27 (cl. 202 only); IEC/EN 60601-2-31 (cl. 202 only); IEC/EN

TÜV Rheinland (Shanghai) Co.,

China, DE

IEC 60601-2-33:2010 + COR1:2012 + A1:2013 + A2:2015 + COR2:2016); German version EN 60601- 2-33:2010 + Cor.:2010 + A11:2011 + A1:2015 + A2:2015 + AC:2016 + A12:2016 Medical Equipment # IEC 60601 -2-37:2024 Medical electrical equip