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

IEC 60601-2-25 Accredited Testing Labs Worldwide

41 accredited laboratories in 9 countries hold IEC 60601-2-25 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.

Total labs
41
Countries
9
Top matrix
Medical equipment, electrical safety and EMC
3 labs

Available in 9 Countries

Germany
14 labs
China
10 labs
United States
8 labs
Canada
2 labs
Japan
2 labs
Taiwan
2 labs
Netherlands
1 lab
Finland
1 lab
Cyprus
1 lab

Top matrices for IEC 60601-2-25

Sample labs

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

IEC 60601-2-25 Edition 2.0 2011-10; ANSI AAMI IEC 60601-2-25:2011/(R)2016; IEC 60601-2-27 Edition 3.0 2011-03; ANSI AAMI IEC 60601-2-27:2011(R)2016; IEC 60601-2-28 Edition 3.0 2017-06; IEC 60601-2-33 Edition 4.0 2022-08; IEC 60601-2-3

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

IEC 60601-2-25; EN 60601-2-25; JIS T 0601-2-25; ANSI AAMI IEC 60601-2-25 (clause 202 only); IEC 60601-2-27; EN 60601-2-27; ANSI AAMI IEC 60601-2-27 (clause 202 only); IEC 60601-2-30; EN 60601-2-30; IEC 80601-2-30 (clause 202 only);

QPS Evaluation Services
Toronto, ON, CA

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 60601-2-40

PRO EMV Labor Strausberg
Strausberg, DE

Prüfgebiet Prüfgegenstand Produkt (Kategorie) Prüfungsart Prüfung Regelwerk Prüfverfahren EMV Medizinprodukte, aktive Prüfung zum Nachweis der Übereinstimmung - Störaussendung - Störfestigkeit DIN EN 60601-1-2 IEC 60601-1-2

TÜV Technische Überwachung Hessen GmbH EMV-Labor
Kassel, DE

IEC 60601-2-25:2011-10 Medical electrical equipment - Part 2-25: Particular requirements for the basic safety and essential performance of electrocardiographs IEC 60601-2-25:1993-03⊗ - Medical electrical equipment - Part 2- 25: Particul

TÜV Rheinland LGA Products
Nürnberg, DE

IEC 60601-2-25:1993 + A1:1999); Deutsche Fassung EN 60601-2-25:1995 + A1:1999 Medizinische elektrische Geräte — Teil 2-26: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Elektroenzephalograph

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 60601-2-25 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-27 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-47 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-50 (Cl 201.17, 202); ANSI/AAMI/IEC 80601-2-30 (Cl 201.17, 202); ANSI/AAMI/IEC 80601-2-35 (Cl 2

VDE Prüf- und Zertifizierungsinstitut
Offenbach am Main, DE

IEC 60601-2-25:1993 + A1:1999); Deutsche Fassung EN 60601-2-25:1995 + A1:1999 VDE 0750-2-25:2001-04 DIN EN 60601-2-26 : 2016-02 Medizinische elektrische Geräte - Teil 2 -26: Besondere Festlegungen für die Sicherheit einschließlich der w

TUV SUD Canada
Gormley, ON, CA

IEC 60601-2-25 Edition 2.0 2011-10; ANSI AAMI IEC 60601-2-25:2011/(R)2016; IEC 60601-2-27 Edition 3.0 2011-03; ANSI AAMI IEC 60601-2-27:2011(R)2016; IEC 60601-2-28 Edition 3.0 2017-06; IEC 80601-2-30: Edition 2.0 2018-03; ANSI AAMI IE

CSA Group Bayern
Plattling, DE

IEC 60601-2-25:1993 + A1:1999); Deutsche Fassung EN 60601-2-25:1995 + A1:1999 VDE 0750-2-25:2001-04 DIN EN 60601-2-26 : 2016-02 ⊗ Medizinische elektrische Geräte - Teil 2-26: Beson dere Festlegungen für die Sicherheit einschließlich de

Intertek Testing Services NA
Duluth, GA, US

IEC 60601-2-25 Edition 2.0 2011-10 3-105 ANSI AAMI IEC 60601-2-25:2011/(R)2016 3-105 IEC 60601-2-27 Edition 3.0 2011-03 3-126 ANSI AAMI IEC 60601-2-27:2011(R)2016 3-126 IEC 60601-2-28 Edition 3.0 2017-06 12-309 IEC 60601-2-33 Ed. 3.2 b

Eurofins Electrical Testing Service (Shenzhen) Co.,
Shenzhen City, Guangdong, CN

IEC 60601-2-25 Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment [Including: Corrigendum 1 (2012)] IEC/EN 60601-2-27; ANSI AAMI IEC 60601-2-27 Part 2-2: P

Shenzhen Huatongwei International Inspection Co.,
Shenzhen, CN

IEC 60601-2-25 Edition 2.0 2011-10 3-105

MedTech Testing Solution Co.,
New Taipei City, TW

IEC 60601-2-25; EN 60601-2-25; BS EN 60601-2-25; CAN/CSA C22.2 No. 60601-2-25; AS/NZS IEC 60601.2.25; JIS T 0601-2-25; ANSI AAMI IEC 60601-2-25 Electrocardiographic monitoring equipment IEC 60601-2-27; EN 60601-2-27; BS EN 6060

UL LLC
Novi, MI, US

IEC 60601-2-25 Edition 2.0 2011-10 (clause 202 only) 3-105 IEC 60601-2-27 Edition 3.0 2011-03 (clause 202 only) 3-126 IEC 60601-2-31 Edition 2.1 2011-09 (clause 202 only) 3-102 IEC 60601-2-33 Ed. 3.2 b:2015 (clause 202 only) 12-295 IEC

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

IEC 60601-2-25; EN 60601-2-25; CSA C22.2 NO. 60601-2-25; ANSI AAMI IEC 60601-2-25

Element Materials Technology Straubing GmbH Element Materials Technology Straubing
Straubing, DE

IEC 60601-2-25 : 2011-10 Medical electrical equipment - Part 2-25: Particular requirements for basic safety and essential performance of electrocardiographs IEC 60601-2-25 : 1993-03 + A1 : 1999-05⊗ - Medical electrical equipment - Part 2

SGS Taiwan
Taoyuan City, TW

IEC 60601-2-25; EN 60601-2-25; ANSI/AAMI 60601-2- 25; CAN/CSA C22.2 No. 60601-2-25; JIS T 0601-2-25 Electrocardiographic monitoring equipment IEC 60601-2-27; EN 60601-2-27; ANSI/AAMI 60601-2- 27; CAN/CSA C22.2 No. 60601-2-27 X-ray

TÜV SÜD Product Service
Frankfurt/Main, DE

IEC 60601-2-25:2011); Deutsche Fassung EN 60601-2-25:2015 VDE 0750-2-25:2001-04 DIN EN 60601-2-25 : 2001-04⊗ - Medizinische elektrische Geräte - Teil 2-25: Besondere Festlegungen für die Sicherheit von Elektro- kardiographen (IEC 60601-2

Eurofins Product Service
Reichenwalde, DE

IEC 60601-2-25 : 2011-10 Medical electrical equipment - Part 2-25: Particular requirements for basic safety and essential performance of electrocardiographs IEC 60601-2-25 : 1993-03 ⊗ - Medical electrical equipment; part 2: particular re

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

IEC 60601-2-25; EN 60601-2-25; ANSI/AAMI 60601-2-25; CAN/CSA C22.2 No. 60601-2-25; IEC 80601-2-26; EN 80601-2-26; CAN/CSA C22.2 No. 80601-2-26; IEC 60601-2-27; EN 60601-2-27; ANSI/AAMI 60601-2-27; CAN/CSA C22.2 No. 60601-2-27;

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

IEC 60601-2-25; EN 60601-2-25; ANSI/AAMI/IEC 60601-2-25; CAN/CSA C22.2 No. 60601-2-25 Medical electrical equipment – Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs IEC 8

TUV Rheinland (Shanghai) Co.,
Shanghai, CN

IEC 60601-2-25; EN 60601-2-25; DIN EN 60601-2-25; VDE 0750-2-25; IEC 60601-2-25 Edition 2.0 2011-10; ANSI AAMI IEC 60601-2-25:2011/(R)2016 Medical electrical equipment −Part 2-25: Particular requirements for basic safety and essen

ITL - International Testing Laboratories (CY)
Limassol, CY

Certification Scheme Product Type / Category Standards / Requirements ITL Certification Scheme Medical Electrical Equipment (MED) (continued) IEC/EN/CAN/SI 60601-2-62; IEC/EN/CAN/SI 60601-2-63; IEC/EN/CAN/SI 60601-2-64; IEC/EN/C

Intertek Testing Services NA
Kentwood, MI, US

IEC 60601-2-25; IEC 60601-2-25 Edition 2.0 2011-10; IEC 60601-2-27; IEC 60601-2-27 Edition 3.0 2011-03; IEC 60601-2-36; IEC 60601-2-36 Edition 2.0 2014-04; IEC 60601-2-37; IEC 60601-2-37 Edition 2.1 2015; IEC 60601-2-37 Edition 3.0

F2 Labs
Middlefield, OH, US

IEC 60601-2-25 Edition 2.0 2011-10 1; ANSI AAMI IEC 60601-2-25:2011/(R)2016 1; ANSI AAMI IEC 60601-2-25 Edition 2.0 2011-10 (Section(s) 201.17/202); ANSI AAMI IEC 60601-2-27:2011(R)2016 1; IEC 60601-2-28 Edition 2.0 2010-03 (Section(s

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

IEC 60601-2-25 : 2011-10 IEC 60601-2-26 : 2012-050 IEC 60601-2-31 : 2020 IEC 60601-2-33 : 2010-03 K DAkkS Deutsche Akkreditierungsstelle Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential pe

TUV Rheinland of North America
Pleasanton, CA, US

IEC 60601-2-25 (Electrocardiographs); EN/IEC 60601-2-26 (Electroencephalographs); EN/IEC 60601-2-27 (Electrocardiographic Monitoring Equipment); EN/IEC 60601-2-28 (X-ray Tube Assembly for Medical Diagnostics); IEC 60601-2-30 (Automatic

cetecom advanced
Saarbrücken, DE

Leistungsmerkmale von endoskopischen Geräten (IEC 60601 -2- 18:2009); Deutsche Fassung EN 60601-2-18:2015 DIN EN 60601-2-25 : 2016-08 Medizinische elektrisch e Geräte - Teil 2-25: Besondere Festlegungen für die Sicherheit einschließlich d

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

SLG Prüf- und Zertifizierungs
Hartmannsdorf, DE

IEC 60601-2-25 - ECG monitoring DIN EN 60601-2-27 IEC 60601-2-27 - non-invasive blood pressure monitors - without testing for measurement accuracy DIN EN ISO 81060-1 DIN EN 1060-1 ⊗ DIN EN 1060-3⊗ - Pulse oximetry devices

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

IEC 60601-2-25 3-105 ANSI AAMI IEC 60601-2-25 3-105 IEC 60601-2-27 3-126 ANSI AAMI IEC 60601-2-27 3-126 IEC 60601-2-34 3-115 IEC 60601-2-36 9-119 IEC 60601-2-37 12-293 IEC 60601-2-47 3-155 ANSI AAMI IEC 60601-2-47 3-155 IEC 61010-1

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 -2-22:2015 VDE 0750-2-22:2015 Medica

SGS Fimko
Helsinki, FI

IEC 60601-2-25; ANSI/AAMI/IEC 60601-2-25

Kiwa Primara
Kaufbeuren, DE

IEC 60601-2-25:1993 + A1:1999); Deutsche Fassung EN 60601-2-25:1995 + A1:1999 VDE 0750-2-25 : 2001-04 ⊗ DIN EN 60601-2-26 : 2016-02⊗ Medizinische elektrische Geräte – Teil 2-26: Beson dere Festlegungen für die Sicherheit einschließlich

TUV Rheinland (Shenzhen) Co.,
Shenzhen, CN

IEC 60601-2-25 Edition 2.0 2011-10; ANSI/AAMI IEC 60601-2-25:2011/(R)2016 3-105 IEC 60601-2-27 Edition 3.0 2011-03; ANSI/AAMI IEC 60601-2-27:2011(R)2016 3-126 IEC 60601-2-28 Edition 3.0 2017-06 12-309 IEC 60601-2-33 Edition 4.0 2022-

TUV SUD Japan
Tokyo, JP

IEC 60601-2-25:2011 (Excluding Section 202); EN 60601-2-25:2015 (Excluding Section 202); JIS T 0601-2-25:2014 (Excluding Section 202);

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 60601-2-25 Edition 2.0, 2011-10 3-105 ANSI AAMI IEC 60601-2-25:2011/(R)2016 3-105 IEC 60601-2-27 Edition 3.0 2011-03 3-126 ANSI AAMI IEC 60601-2-27:2011(R)2016 3-126 IEC 60601-2-47 Edition 2.0 2012-02 3-155 ANSI AAMI IEC 60601-2-47

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

IEC 60601-2-25, Clause 202 of EN 60601-2-25, Clause 202 of IEC 60601-2-27, Clause 202 of EN 60601-2-27, Clause 202 of IEC 80601-2-30, Clause 202 of EN IEC 80601-2-30, Clause 202 of IEC 60601-2-37, Clause 202 of EN 60601-2-37,