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

IEC 60601-2-18 Accredited Testing Labs Worldwide

52 accredited laboratories in 7 countries hold IEC 60601-2-18 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle. In the register, IEC 60601-2-18 scope entries most often cover Radiation, Ionizing/Non-Ionizing in Medical equipment, electrical safety and EMC, Electrical equipment.

Total labs
52
Countries
7
Top matrix
Medical equipment, electrical safety and EMC
5 labs

Available in 7 Countries

Germany
19 labs
China
17 labs
United States
10 labs
Japan
3 labs
Canada
2 labs
Taiwan
2 labs
Italy
1 lab

Top matrices for IEC 60601-2-18

Medical equipment, electrical safety and EMC
5 labs
Electrical equipment
1 lab

Top analytes for IEC 60601-2-18

  • Radiation, Ionizing/Non-Ionizing (1)

Sample labs

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

IEC 60601-2-18; IEC 60601-2-22; IEC 60601-2-28 2; IEC 60601-2-36; 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 6

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

IEC 60601-2-18 : 2009-08 Medical electrical equipment - Part 2-18: Particular requirements for basic safety and essential performance of endoscopic equipment IEC 60601-2-23 : 2011-02 Medical electrical equipment - Part 2-23: Particular r

UL International Germany
Neu-Isenburg, DE

Leistungsmerkmale von Geräten zur Stimulation von Nerven und Muskeln (IEC 60601-2-10:2012 + A1:2016); Deutsche Fassung EN 60601-2-10:2015 + A1:2016 DIN EN 60601-2-18 : 2016-10 Medizinische elektrisch e Geräte - Teil 2-18: Besondere Fes

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

IEC 60601-2-18: Edition 3.0 2009-08; IEC 60601-2-19 Edition 3.0 2020-09; IEC 60601-2-20 Edition 3.0 2020-09; IEC 60601-2-21 Edition 3.0 2020-09; IEC 60601-2-22 Edition 4.0 2019-11; IEC 60601-2-25 Edition 2.0 2011-10; ANSI AAMI IEC 606

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

Test: Test Method(s)1: EMC – Medical Equipment (continued) EN 60601-2-18 (clause 202 only); IEC 60601-2-21; EN IEC 60601-2-21; JIS T 0601-2-21 (clause 202 only); IEC 60601-2-22; EN IEC 60601-2-22; JIS T 0601-2-22 (clause 202 onl

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

IEC 60601-2-18; IEC 60601-2-18 Edition 3.0 2009-08; CSA C22.2 No. 60601-2-18; EN 60601-2-18 IEC 60601-2-2; IEC 60601-2-2 Edition 6.0 2017-03; IEC 60601-2-2:2017/A1:2023; ANSI AAMI IEC 60601-2-2; ANSI AAMI IEC 60601-2-2:2017; CSA

QPS Evaluation Services
Toronto, ON, CA

IEC 60601-2-18; IEC 60601-2-2; IEC 60601-2-23; 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

Intertek Japan K.K.
Tokyo, JP

IEC 60601-2-18; EN 60601-2-18; IEC 60601-2-18: Edition 3.0 2009-08; IEC 60601-2-28 (Ed 2, Ed 3); IEC 60601-2-28 Edition 3.0 2017-06;

PRO EMV Labor Strausberg
Strausberg, DE

Quellenverzeichnis Regelwerke/Prüfverfahren: DIN EN 60601-1-2:2022-01 Medizinische elektrische Geräte - Teil 1-2: Allgemeine Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale - Ergänzungsnorm: Elektromagn

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

IEC 60601-2-18; EN 60601-2-18; CSA C22.2 NO. 60601-2-18 IVD (In Vitro Diagnostic Medical Devices): IEC 61010-1; EN 61010-1; CAN/CSA-C22.2 NO. 61010-1; UL 61010-1; IEC 61010-2-010; EN IEC 61010-2-010; CAN/CSA-C22.2 No. 61010-2-010; UL

TÜV Technische Überwachung Hessen GmbH EMV-Labor
Kassel, DE

IEC 60601-2-18:2009-08 Medical electrical equipment - Part 2-18: Particular requirements for the basic safety and essential performance of endoscopic equipment. IEC 60601-2-23:2011-02 Medical electrical equipment - Part 2-23: Particular

TÜV Rheinland LGA Products
Nürnberg, DE

DIN EN 60601-2-5 : 2016-08 DAkkS Deutsche Akkreditierungsstelle der wesentlichen Leistungsmerkmale von Defibrillatoren (IEC 60601-2-4:2010); Deutsche Fassung EN 60601-2-4:2011 Medizinische elektrische Geräte - Teil 2-5: Besondere Festlegung

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 -2-10:2012 + A1:2016 IEC 60601-2- 10:201

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

Test Technology: Test Method(s) 2,3: Medical Equipment (cont.) ISO 80601-2-84 (Cl 201.17, 202); ISO 80601-2-85 (Cl 201.11.6.5, 201.15.3.5.1

VDE Prüf- und Zertifizierungsinstitut
Offenbach am Main, DE

IEC 60601-2-18 : 2009-08 Medical electrical equipment - Part 2-18: Particular requirements for basic safety and essential performance of endoscopic equipment IEC 60601-2-18 : 1996-08⊗ - Medical electrical equipment - Part 2: Particular

TUV SUD Canada
Gormley, ON, CA

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 4.0 2019-11; IEC 60601-2-23 Edition 3.0 2011-02; IEC 60601-2-25 Ed

CSA Group Bayern
Plattling, DE

IEC 60601-2-18:1996 + A1:2000); Deutsche Fassung EN 60601-2-18:1996 + A1:2000 VDE 0750-2-18:2001-12 ⊗ DIN EN IEC 60601-2-19 : 2022-08 ⊗ Medizinische elektrische Geräte - Teil 2 -19: Besondere Festlegungen für die Sicherheit einschli

Intertek Testing Services NA
Duluth, GA, US

IEC 60601-2-18: Edition 3.0 2009-08 9-114 IEC 60601-2-19 Edition 3.0 2020-09 6-461 IEC 60601-2-21 Edition 3.0 2020-09 6-463 IEC 60601-2-22 Edition 3.1 2012-10 12-268 IEC 60601-2-22 Edition 4.0 2019-11 12-356 IEC 60601-2-23 Edition 3.0

Device Conformity and Testing
Devens, MA, US

IEC 60601-2-18:2009-08

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

Test Technology: Test Method(s) 2,3,4: Part 1-11: General requirements for basic safety and essential performance -- Collateral Standard: Requirements for medical electrical equipment and medical electrical equipment and medical ele

Shenzhen Huatongwei International Inspection Co.,
Shenzhen, CN

IEC 60601-2-18 Edition 3.0 2009-08 9-114 IEC 60601-2-22 Edition 3.1 2012-10 12-268 IEC 60601-2-25 Edition 2.0 2011-10 3-105

MedTech Testing Solution Co.,
New Taipei City, TW

IEC 60601-2-18; EN 60601-2-18; BS EN 60601-2-18; CAN/CSA C22.2 No. 60601-2-18; AS/NZS IEC 60601.2.18; JIS T 0601-2-18 Surgical, cosmetic, therapeutic and diagnostic laser equipment IEC 60601-2-22; EN IEC 60601-2-22; BS EN IEC 6

NEMKO
Pfinztal, DE

IEC 60601-2-18:1996 + A1:2000); Deutsche Fassung EN 60601-2-18:1996 + A1:2000 VDE 0750-2-18:2001-12

UL LLC
Novi, MI, US

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 IEC 60601-2-21 Edition 3.0 2020-09 (clause 202 only) 6-463

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

IEC 60601-2-18; EN 60601-2-18; CSA-C22.2 No. 60601-2-18 Medical electrical equipment – Part 2-19: Particular Requirements for the Basic Safety and Essential Performance of Infant Incubators IEC 60601-2-19; EN IEC 60601-2-19; ANSI

Shenzhen CTL Testing Technology Co.,
Shenzhen, CN

IEC 60601-2-18; EN 60601-2-18

Element Materials Technology Fremont Newark
Fremont, CA, US

Test: Test Method(s) 1: Generic and Product Family Standards (cont.) IEC 62236-4; EN 50155; EN 55013; KN 13; EN 55020 (only for audio/video equipment without tuner); KN 20 (only for audio/video equipment without tuner); EN 50

SGS Taiwan
Taoyuan City, TW

IEC 60601-2-18; EN 60601-2-18; CAN/CSA-C22.2 No. 60601-2-18 Surgical, cosmetic, therapeutic and diagnostic laser equipment IEC 60601-2-22; EN IEC 60601-2-22; CAN/CSA-C22.2 No. 60601-2-22 Electrocardiographs IEC 60601-2-25; E

TÜV SÜD Product Service
Frankfurt/Main, DE

IEC 60601-2-18:2009); Deutsche Fassung EN 60601-2-18:2015 VDE 0750-2-18 : 2016-10 DIN EN 60601-2-18 : 2001-12⊗ - Medizinische elektrische Geräte - Teil 2-18: Besondere Festlegungen für die Sicherheit von endoskopischen Geräten (IEC 6060

Eurofins Product Service
Reichenwalde, DE

IEC 60601-2-18 : 2009-08 Medical electrical equipme nt - Part 2-18: Particular requirements for basic safety and essential performance of endoscopic equipment IEC 60601-2-18 : 1996-08 ⊗ - Medical electrical equipment - Part 2: Particul

Intertek Deutschland
Kaufbeuren, DE

IEC 60601-2-18:1996 + A1:20 00); Deutsche Fassung EN 60601-2-18:1996 + A1:2000 VDE 0750-2-18:2001-12 ⊗ DIN EN IEC 60601 -2-22 : 2022 -10 Medizinische elektrische Geräte - Teil 2 -22: Besondere Festlegungen für die Sicherheit einschlie

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

IEC 60601-2-18; EN 60601-2-18; CAN/CSA-C22.2 No. 60601-2-18; IEC 60601-2-28; EN 60601-2-28; CSA C22.2 NO. 60601-2-28; IEC 60601-2-44; EN 60601-2-44; CAN/CSA-C22.2 No. 60601-2-44; IEC 60601-2-45; EN 60601-2-45; CAN/CSA-C22.2

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

IEC 60601-2-18; EN 60601-2-18; CAN/CSA-C22.2 No. 60601-2-18 Medical electrical equipment – Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment

TUV Rheinland (Shanghai) Co.,
Shanghai, CN

IEC 60601-2-18; EN 60601-2-18; DIN EN 60601-2-18; VDE 0750-2-18; IEC 60601-2-18: Edition 3.0 2009-08 Medical electrical equipment − Part 2-18: Particular requirements for basic safety and essential performance of endoscopic equipmen

Intertek Testing Services NA
Kentwood, MI, US

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 2011-10; IEC 60601-2-27; IEC 60601-2-27 Edition 3.0

F2 Labs
Middlefield, OH, US

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 (Section(s) 201.17/202) 1

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

IEC 60601-2-18:2009); Deutsche Fassung EN 60601-2-18:2015 VDE 0750-2-18 : 2016-10 DIN EN 60601-2-18 : 2001-120- Medizinische elektrische Geräte -Tell 2-18: Besondere Festlegungen für die Sicherheit von endoskopischen Geräten (IEC 60601-2-18

TUV Rheinland of North America
Pleasanton, CA, US

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 Edition 2.1 2016-04 6-462 IEC 60601-2-21 Edition 2.1 2016-04 6-463 IEC 60601-2-22 Edition 3.1 2012-10 12-268 IEC 60601-2-22

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

DEKRA Testing and Certification (Suzhou) Co.,
Suzhou, Jiangsu Province, CN

IEC 60601-2-18; EN 60601-2-18; CAN/CSA-C22.2 No. 60601-2-18 Medical electrical equipment – Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers IEC 80601-2-30; EN

TUV Rheinland (China)
Beijing, CN

IEC 60601-2-18: Edition 3.0 2009-08 9-114 IEC 60601-2-22 Edition 4.0 2019-11 (excluding clauses listed in the “Exclusion” table above) 12-356 IEC 60601-2-37 Edition 2.1 2015 (excluding clauses listed in the “Exclusion” table above)

SLG Prüf- und Zertifizierungs
Hartmannsdorf, DE

IEC 60601-2-18 - HF surgical devices and accessories DIN EN 60601-2-2 IEC 60601-2-2 Ophthalmic devices Checking compliance with general and specific requirements - Devices for lens and vitreous removal DIN EN 80601-2-58 I

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

IEC 60601-2-18;

Sigma Scientific Services
Sunrise, FL, US

IEC 60601-2-18 Edition 3.0 2009-08 Photobiological safety of lamps and lamp systems IEC 62471 Edition 1.0 b:2006 Exclusion: Wavelength range 1100nm - 3000nm Ophthalmic Instruments Ophthalmic instruments – Fundamental Requiremen

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 -2-16:2016 VDE 0750-2-16:2016 Medical

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

White Lab S.r.l. - Test'ing
Falconara Marittima, IT

White Lab S.r.l. - Test'ing Via del Consorzio, 41 60015 Falconara Marittima AN Allegato al certificato di accreditamento n. 01044 rev. 7 del 21/05/2025 UNI CEI EN ISO/IEC 17025:2018 Revisione: 25 Sede A Data: 21/05/2025 pag. 4 d

TUV Rheinland (Shenzhen) Co.,
Shenzhen, CN

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 60601-2-20 Edition 3.0 2020-09 6-462 IEC 60601-2-22 Edition 4.0 2019-11; IEC

TUV SUD Japan
Tokyo, JP

IEC 60601-2-18:1996 + A1:2000; IEC 60601-2-18:2009; EN 60601-2-18:1996 + A1:2000; JIS T 0601-2-18:2005; JIS T 0601-2-18:2013; CAN/CSA-C22.2 No. 60601-2-18:11 (R2021); IEC 60601-2-5:2000 (Only Sections, 50, 51.5, 51.104); EN 60601-2

TÜV NORD CERT
Essen, DE

IEC 60601-2-18:2009); Deutsche Fassung EN 60601-2-18:2015 DIN EN IEC 61326 -2-6 2022-11 Elektrische Mess -, Steuer -, Regel- und Laborgeräte - EMV - Anforderungen - Teil 2-6: Besondere Anforderungen - Medizinische In-vitro-Diagnoseg

Showing labs 1–50 of 52. Use pagination below to see more.