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

IEC 60601-2-37 Accredited Testing Labs Worldwide

40 accredited laboratories in 6 countries hold IEC 60601-2-37 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.

Total labs
40
Countries
6
Top matrix
Medical equipment, electrical safety and EMC
4 labs

Available in 6 Countries

China
13 labs
Germany
13 labs
United States
10 labs
Japan
3 labs
Taiwan
2 labs
Canada
1 lab

Top matrices for IEC 60601-2-37

Medical equipment, electrical safety and EMC
4 labs
Electrical equipment
1 lab
Water
1 lab

Sample labs

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

IEC 60601-2-37; 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;

E & C Testlab GmbH (Engineering & Certification Testlab GmbH)
Trossingen, DE

IEC 60601-2-37 : 2007-08 Medical electrical equipment - Part 2-37: Particular requirements for the basic sa fety and essential performance of ultrasonic medical diagnostic and monitoring equipment + Amendment 1 : 2015-06

TUV SUD Certification and Testing (China) Co.,
Wuxi, CN

IEC 60601-2-37 Edition 2.1 2015; IEC 60601-2-37 Edition 3.0 2024-07; IEC 60601-2-40 Third edition 2024-12; 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;

TUV SUD Japan Ltd. Yonezawa Testing Center (EMC Lab)
Yamagata, JP

IEC 60601-2-37; EN 60601-2-37; JIS T 0601-2-37; IEC 60601-2-37:2007 + AMD1:2015 (clause 202 only); IEC 60601-2-39; EN IEC 60601-2-39; JIS T 0601-2-39 (clause 202 only); IEC 60601-2-47; IEC 60601-2-47:2012; EN 60601-2-47; ANSI AAMI I

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

IEC 60601-2-37; IEC 60601-2-37 Edition 2.1 2015; IEC 60601-2-37 Edition 3.0 2024-07; CSA C22.2 No. 60601-2-37; EN 60601-2-37 IEC 62359; IEC 62359 Edition 2.1 2017-09 CONSOLIDATED VERSION; EN 62359 IEC 60601-2-57; IEC 60601-2-5

Intertek Japan K.K.
Tokyo, JP

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; IEC 60601-2-44; IEC 60601-2-44 Edition 3.2: 2016; IEC 60601-2-46; IEC 60601-2-52;

Element Materials Technology Portland - Evergreen
Hillsboro, OR, US

Test Technology: Test Method(s) 1, 2: Generic / Product Family / Product Specific Standards (cont.) EN 60601-2-37 (2008) + A1 (2015), clause 202; IEC 60601-2-47 Ed. 2.0 (2012-02), clause 202; IEC 60601-2-49 (2011), clause 202; E

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

IEC 60601-2-37; EN 60601-2-37; CSA C22.2 NO. 60601-2-37; IEC 60601-2-5; EN 60601-2-5; CSA C22.2 NO. 60601-2-5 Dental Device Related Testing: ISO 7494-1; EN ISO 7494-1; ISO 7494-2; EN ISO 7494-2; ISO 9680; EN ISO 9680; ISO 10650; EN I

TÜV Technische Überwachung Hessen GmbH EMV-Labor
Kassel, DE

IEC 60601-2-37:2007-08 Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment + Amendment 1:2015-06 IEC 60601-2-38:1996-

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

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

Test Technology: Test Method(s)2,3: Medical Equipment (cont.) EN 60601-2-336 (Excluding Cl 201.17, 202); EN 60601-2-34 (Excluding Cl 201.17

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. DIN EN 60601-2-37 : 2016-11 Medizinische elektrische Geräte – Teil 2 -37: Besondere Festlegungen für die Sicherheit ei

TUV SUD Canada
Gormley, ON, CA

IEC 60601-2-37 Edition 2.1 2015; 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

CSA Group Bayern
Plattling, DE

IEC 60601-2-37:2007 + A1:2015); Deutsche Fassung EN 60601-2-37:2008 + A11:2011 + A1:2015 VDE 0750-2-37:2016-11 DIN EN 60601-2-37 : 2012-05 ⊗ - Medizinische elektrische Geräte - Teil 2-37: Besondere Festlegungen für die Sicherheit eins

Intertek Testing Services NA
Duluth, GA, US

IEC 60601-2-37 (Ed. 2 + Am 1, Ed. 3) (excluding cl 201.12); IEC 60601-2-38; IEC 60601-2-40 (Ed. 1, Ed. 2, Ed. 3); IEC 60601-2-41 (Ed. 2 + Am 1, Ed. 3); IEC 60601-2-46 (Ed. 3, Ed. 4); IEC 60601-2-49 (Ed. 1, Ed.2); IEC 60601-2-50 (Ed. 2

Shenzhen Huatongwei International Inspection Co.,
Shenzhen, CN

IEC 60601-2-37 Edition 2.1 2015 12-293 IEC 60601-2-47 Edition 2.0 2012-02 3-155 IEC 60601-2-50 Edition 3.0 2020-09 6-450 IEC 60601-2-52 Edition 1.1 2015-03 CONSOLIDATED VERSION 6-489 IEC 60601-2-52 Edition 1.0 2009-12 6-321 IEC 60601-2

MedTech Testing Solution Co.,
New Taipei City, TW

IEC 60601-2-37; EN 60601-2-37; BS EN 60601-2-37; CAN/CSA C22.2 No. 60601-2-37; JIS T 0601-2-37 Peritoneal dialysis equipment IEC 60601-2-39; EN IEC 60601-2-39; BS EN IEC 60601-2-39; CAN/CSA C22.2 No. 60601-2-39; AS/NZS IEC 60601.

UL LLC
Novi, MI, US

IEC 60601-2-37 Edition 2.1 2015 (clauses 201.17, 202 only) 12-293 IEC 60601-2-44 Edition 3.2: 2016 (clause 202 only) 12-302 IEC 60601-2-45 Edition 3.1 2015 (clause 202 only) 12-294 IEC 60601-2-47 Edition 2.0 2012-02 (clause 202 only) 3-1

Eurofins Electrical Testing Service (Shanghai) Co.,
Shanghai, CN

IEC 60601-2-37; EN 60601-2-37; EN IEC 60601-2-37; CSA-C22.2 No. 60601-2-37 Medical Electrical Equipment –Part 2-41: Particular Requirements for the Basic Safety and Essential Performance of Surgical Luminaires and Luminaires for D

SGS Taiwan
Taoyuan City, TW

IEC 60601-2-37; EN 60601-2-37; CAN/CSA-C22.2 No. 60601-2-37 Electromyographs and evoked response equipment IEC 60601-2-40; EN 60601-2-40; CAN/CSA-C22.2 No. 60601-2-40 Operating tables IEC 60601-2-46; EN IEC 60601-2-46; CAN/C

TÜV SÜD Product Service
Frankfurt/Main, DE

IEC 60601-2-37:2007 + A1:2015); Deutsche Fassung EN 60601-2-37:2008 + A11:2011 + A1:2015 DIN EN 60601-2-37 : 2012-05⊗ - Medizinische elektrische Geräte - Teil 2-37: Besondere Festlegungen für die Sicherheit einschließlich der wesentlich

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

IEC 60601-2-37; EN 60601-2-37; CAN/CSA-C22.2 No. 60601-2-37; IEC 60601-2-41; EN 60601-2-41; CAN/CSA-C22.2 No. 60601-2-41; IEC 60601-2-46; EN IEC 60601-2-46; CAN/CSA C22.2 NO. 60601-2-46; IEC 60601-2-47; EN 60601-2-47; ANSI/

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

IEC 60601-2-37; EN 60601-2-37; CAN/CSA-C22.2 No. 60601-2-37 Medical electrical equipment – Part 2-40: Particular requirements for basic safety and essential performance of electromyographs and evoked response equipment IEC 60601-2

TUV Rheinland (Shanghai) Co.,
Shanghai, CN

IEC 60601-2-37; EN 60601-2-37; DIN EN 60601-2-37; VDE 0750-2-37; IEC 60601-2-37 Edition 2.1 2015 Medical electrical equipment − Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires a

Intertek Testing Services NA
Kentwood, MI, US

IEC 60601-2-37; IEC 60601-2-37 Edition 2.1 2015; IEC 60601-2-37 Edition 3.0 2024-07 (The above standards exclude Clause 201.12.4 Acoustic Output); IEC 60601-2-38; IEC 60601-2-39; IEC 60601-2-39 Edition 3.0 2018-04; IEC 606

F2 Labs
Middlefield, OH, US

IEC 60601-2-37 Edition 2.1 2015 (Section(s) 201.17/202) 1; IEC 60601-2-37 Edition 3.0 2024-07; 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)

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

IEC 60601-2-37 : 2007-08 IEC 60601-2-39 : 2018-04 I EC 60601-2-40 : 2016-08 IEC 60601-2-46 : 2016-08 IEC 60601-2-47 : 2012-02 IEC 60601-2-49 : 2011-020 IEC 60601-2-50 : 2020-09 DAkkS Deutsche Akkreditierungsstelle Medical electrical equipme

TUV Rheinland of North America
Pleasanton, CA, US

IEC 60601-2-37 (Ultrasonic Medical Diagnostic and Monitoring Equipment); EN/IEC 60601-2-38 (Electrically Operated Hospital Beds); EN/IEC 60601-2-39 (Peritoneal Dialysis Equipment); EN/IEC 60601-2-40 (Electromyographs and Evoked Response

PHOENIX TESTLAB
Blomberg, DE

IEC 60601-2-37:2007 + A1: 2015); Deutsche Fassung EN 60601-2-37:2008 + A11:2011 + A1:2015 DIN EN 60601-2-37 : 2012-05 ⊗ - Medizinische elektrische Geräte - Teil 2-37: Besondere Festlegungen für die Sicherheit einschließlich der wesentli

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 Korea Ltd. Test Center, Safety of Electrical Appliances and Ergonomics
Republic Of, DE

Department Standard/in house procedure/Version Title of standard or in house procedure (deviations/modifications of standard) Test area/ reductions MED IEC 80601 -2-30:2009 +AMD1:2013 SIST EN 80601-2-30:2010+ +AMD1:2015 IEC 80

TUV Rheinland (China)
Beijing, CN

IEC 60601-2-37 Edition 2.1 2015 (excluding clauses listed in the “Exclusion” table above) 12-293 IEC 60601-2-52 Edition 1.1 2015-03 CONSOLIDATED VERSION (excluding clauses listed in the “Exclusion” table above) 6-489 IEC 61010-1 Ed

SLG Prüf- und Zertifizierungs
Hartmannsdorf, DE

IEC 60601-2-37 Monitoring devices Checking compliance with general and specific requirements - multifunctional patient monitoring devices DIN EN IEC 80601-2-49 DIN EN 60601-2-49 ⊗ IEC 60601-2-49 ⊗ - Devices for monitor

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

IEC 60601-2-37 12-293 IEC 60601-2-47 3-155 ANSI AAMI IEC 60601-2-47 3-155 IEC 61010-1 19-34 ANSI/UL 61010-1 19-41 IEC 80601-2-30 3-123 ANSI AAMI IEC 80601-2-30 3-123 ISO 80601-2-55 1-140 ISO 80601-2-56 6-421 ISO 80601-2-61 1-139 I

Sigma Scientific Services
Sunrise, FL, US

IEC 60601-2-37 Edition 2.1 2015 12-293 IEC 60601-2-5 Edition 3.0 2009-07 12-205 IEC 60601-2-62 Edition 1.0 2013-07 12-281

Bay Area Compliance
Sunnyvale, CA, US

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) [Incl. AMD2:2021]; EN 60601-1-2 (2001+A1:2006,

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

SHENZHEN STS TEST SERVICES CO.,LTD.
Shenzhen, CN

Test Technology: Test Method(s): Product Safety (Cont’d) AS/NZS 60669.1 (excluding: 22.5, 25); IEC/EN 60669-2-1 (excluding: 22.5, 25); BS

TUV SUD Japan
Tokyo, JP

IEC 60601-2-37:2001 + A1:2004 + A2:2005; JIS T 0601-2-37:2005; IEC 60601-2-37:2007 (Excluding Section 202); IEC 60601-2-37:2007 + A1:2015 (Excluding Section 202); EN 60601-2-37:2008 (Excluding Section 202); JIS T 0601-2-37:2013 (Ex

TUV SUD Certification and Testing (China) Co., Ltd. Shenzhen Branch
Shenzhen, CN

IEC 60601-2-37, Clause 202 of EN 60601-2-37, Clause 202 of IEC 80601-2-49, Clause 202 of EN IEC 80601-2-49, Clause 202 of ISO 80601-2-55, Clause 202 of EN ISO 80601-2-55, Clause 202 of ISO 80601-2-56, Clause 202 of EN ISO 80601-2