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

IEC 61010-2-101 Accredited Testing Labs Worldwide

43 accredited laboratories in 11 countries hold IEC 61010-2-101 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle, Italian Accreditation Body. In the register, IEC 61010-2-101 scope entries most often cover Blood-Glucose in Medical equipment, electrical safety and EMC, Electrical equipment, Measuring Equipment.

Total labs
43
Countries
11
Top matrix
Medical equipment, electrical safety and EMC
4 labs

Available in 11 Countries

Germany
15 labs
China
10 labs
United States
7 labs
Italy
3 labs
Japan
2 labs
Taiwan
2 labs
Finland
2 labs
Sweden
1 lab
South Korea
1 lab
Canada
1 lab
United Kingdom
1 lab

Top matrices for IEC 61010-2-101

Top analytes for IEC 61010-2-101

  • Blood-Glucose (1)

Sample labs

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

IEC 61010-2-101; EN 61010-1; EN IEC 61010-2-010; EN IEC 61010-2-011; EN 61010-2-020; EN IEC 61010-2-030; EN IEC 61010-2-040; EN IEC 61010-2-051; EN IEC 61010-2-081; EN IEC 61010-2-091; EN IEC 61010-2-101; ANSI UL 61010-1; CAN/CS

UL International Germany
Neu-Isenburg, DE

IEC 61010-2-101:2015); Deutsche Fassung EN 61010-2-101:2017 (in Verbindung mit DIN EN 61010-1 : 2011-07, solange eine gültige Akkreditierung hierfür besteht) IEC 60601-1 : 2005-12 Medical electrical equipment - Part 1: General requireme

TUV ITALIA
Volpiano, IT

TUV ITALIA SrL Via Brandizzo 123 10088 Volpiano TO Allegato al certificato di accreditamento n. 00077 rev. 7 del 23/01/2025 UNI CEI EN ISO/IEC 17025:2018 Revisione: 10 Sede B Data: 19/03/2025 pag. 2 di 62 Par 04 - Prove in cond

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

IEC 61010-2-101; IEC 61010-2-101 Edition 3.0 2018-10; CSA C22.2 NO. 61010-2-101; EN IEC 61010-2-101 ISO 18113-5; ISO 18113-5 Edition 2 2022-10; EN ISO 18113-5 EN 1789; EN 1789:2020; EN 1789:2020+A1:2023 ISO 27427; ISO 27427 T

QPS Evaluation Services
Toronto, ON, CA

IEC 61010-2-101; IEC 61010-2-201; IEC 62471; IEC 62471-5; ISA 82.02.01; UL 1436; UL 61010-1; UL 61010-2-010; UL 61010-2-011; UL 61010-2-020; UL 61010-2-031; UL 61010-2-032; UL 61010-2-041; UL 61010-2-042; UL 61010-2-051; UL 6

Intertek Japan K.K.
Tokyo, JP

IEC 61010-2-101 MED, Medical (excluding Resistance to Environment Stress, Cathode Ray Tubes, Lasers and Light Emitting Diodes, Primary Lithium Batteries, Protection against Hazards of Ignition of Flammable Anesthetics Mixtures, Simu

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

IEC 61010-2-101; EN IEC 61010-2-101; CAN/CSA-C22.2 No. 61010-2-101; UL 61010-2-101 Biocompatibility Testing: ISO 10993-12; ISO 10993-18 SGS-CSTC STANDARDS TECHNICAL SERVICES CO., LTD. GUANGZHOU BRANCH Room 101, Building 3, No. 1501

TÜV Rheinland LGA Products
Nürnberg, DE

IEC 61010-2-101:2015); Deutsche Fassung EN 61010-2-101:2017 (in Verbindung mit DIN EN 61010-1 : 2011-07, solange eine gültige Akkreditierung hierfür besteht) DIN EN 61010-2-101 : 2003-090 - Sicherheitsbestimmungen für elektrische Mess-, Ste

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 61010 -2-040:2020 EN 61010-2-040:2021 DIN EN 6

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

IEC 61010-2-1016; EN 61010-2-1016; EN IEC 61010-2-1016; CSA C22.2 No. 61010-2-1016; ANSI/UL 61010-2-1016; IEC 61010-2-130; EN IEC 61010-2-130; BS EN IEC 61010-2-130; IEC 61010-2-201; EN IEC 61010-2-201; BS EN IEC 61010-2-201; UL 6101

TUV SUD America
Alpharetta, GA, US

IEC 61010-2-101:2015; IEC 61010-2-101:2018; UL/CSA 61010-2-101:2019; EN 61010-2-101:2017; EN IEC 61010-2-101:20222/A11:2022; UL/EN/CSA 61010-2-101; UL 61010-2-051:2019; EN IEC 61010-2-051:2021/A11:2021; CAN/CSA-C22.2 No. 61010-2-

VDE Prüf- und Zertifizierungsinstitut
Offenbach am Main, DE

IEC 61010-2-101:2015 DIN EN 61010-2-101:2013 VDE 0411-2-101:2013 Sicherheitsbestimmungen für elektrische Mess-, Steuer-, Regel- und Laborgeräte - Teil 2-101: Besondere Anforderungen an In-vitro-Diagnostik- (IVD-)Medizingeräte A IEC

CSA Group Bayern
Plattling, DE

IEC 61010-2-101:2015); Deutsche Fassung EN 61010-2-101:2017 (in Verbindung mit DIN EN 61010-1 : 2011-07, solange eine gültige Akkreditierung hierfür besteht) DIN EN 61010-2-101 : 2003-09 ⊗ - Sicherheitsbestimmungen für elektrische Mes

KEYMKR
Lübeck, DE

IEC 61010-2-101:2015); Deutsche Fassung EN 61010-2-101:2017 VDE 0411-2-101:2017-10 (in Verbindung mit DIN EN 61010-1:2011-07, (solange eine gültige Akkreditierung hierfür besteht) DIN EN ISO 11197 : 2020-05 Medizinische Versorgungseinhe

Intertek Testing Services NA
Duluth, GA, US

IEC 61010-2-101 (Ed. 2, Ed. 3); IEC 61010-2-201 (Ed. 1, Ed. 2) Audio/Video (excluding Vicat Softening, CRT/High Vacuum, and Annex H Insulating Winding Wires) IEC 60065; EN 60065; UL 60065; CSA C22.2 No. 60065 Household (ex

Device Conformity and Testing
Devens, MA, US

IEC 61010-2-101:2018 Testing Activities performed under the scope of the U.S FDA ASCA Pilot Program Specifications: Basic Safety and Essential Performance of Medical Electrical Equipment, Medical Electrical Systems, and Laboratory Medi

RISE Research Institutes of Sweden
Lund, SE

Datum 2026-02-19 2026/274 Säkerhetsprovning Elsäkerhet Metod Parameter Provtyp Flex Typ av flex Fält Anmärkning SS-EN 61010-2-030 Laboratorieutrustning Ja 2 Nej SS-EN 61010-2-081 Laboratorieutrustning Ja 2 Nej SS-EN 61010-2-101 Laboratori

TÜV Rheinland Japan Ltd. Kansai Technology Center Osaka
Japan, DE

Department Standard/in house procedure/ Version Title of standard or in house procedure (deviations/modifications of standard) Test area/ reductions Product Safety * IEC 61010 -031:2015 + A1:2018 EN 61010-031:2015 + A1:2021 + A

MedTech Testing Solution Co.,
New Taipei City, TW

IEC 61010-2-101; EN IEC 61010-2-101; BS EN IEC 61010-2-101; ANSI/UL 61010-2-101; CAN/CSA C22.2 No. 61010-2-101; JIS C 1010-2-101 On the following products or types of products: Medical Electrical Equipment and Laboratory Equ

Etteplan Finland Oy, Test
Jyväskylä, FI

T298/M23/2025 Liite 1 / Appendix 1 Sivu / Page 23(23) Vaatimus/Requirement SFS-EN ISO/IEC 17025:2017 17.12.2025 Päätöksen päiväys / Date of decision 22.07.2028 Päätöksen viimeinen voimassaolopäivä / Date of expiry www.finas.fi Voimas

NEMKO
Pfinztal, DE

IEC 61010-2-101:2015); Deutsche Fassung EN 61010-2-101:2017 VDE 0411-2-101 : 2017-10 DIN EN 61010-2-101 : 2003-09 ⊗ - Sicherheitsbestimmungen für elektrische Mess-, Steuer-, Regel- und Laborgeräte - Teil 2-101: Besondere Anforderungen

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

IEC 61010-2-101; EN 61010-2-101; EN IEC 61010-2-101; UL 61010-2-101; CSA C22.2 NO. 61010-2-101 Explosive Equipment Explosive Atmospheres IEC 60079-0; EN IEC 60079-0; UL 60079-0; CAN/CSA-C22.2 No. 60079-0 Part 1: Equipment P

Shenzhen CTL Testing Technology Co.,
Shenzhen, CN

IEC 61010-2-101; EN IEC61010-2-101 Medical electrical equipment - Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment IEC 80601-2-49; EN IEC 80601-2-49

SGS Taiwan
Taoyuan City, TW

IEC 61010-2-101; EN IEC 61010-2-101; CSA C22.2.61010-2-101; UL 61010-2-101; BS EN 61010-2- 101 Control equipment IEC 61010-2-201; EN 61010-2-201; CSA C22.2.61010- 2-201; UL 61010-2-201 Requirements for blood-glucose monitoring sy

TÜV SÜD Product Service
Frankfurt/Main, DE

IEC 61010-2-101:2015); Deutsche Fassung EN 61010-2-101:2017 (in Verbindung mit DIN EN 61010-1 : 2020-03, solange eine gültige Akkreditierung hierfür besteht) DIN EN 61010-2-101 : 2017-10⊗ - Sicherheitsbestimmungen für elektrische Mess-

Eurofins Product Service
Reichenwalde, DE

IEC 61010-2-101 : 2015-01 ⊗ Safety requirements for electrical equipment for m easurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment (in conjunction with IEC 61010-1

Eurofins Electrical & Electronic UK
North Yorkshire, GB

IEC 61010-2-101:2015 C, G medical equipment EN 61010-2-101:2017 C, G IEC 61010-2-101: 2018 C, G EN IEC 61010-2-101:2022 +A11: 2022 C, G Excluding: 7.203 Vibration testing – ISO349-1

Intertek Deutschland
Kaufbeuren, DE

IEC 61010-2-101 : 2023-12 Sicherheitsbestimmungen für elektrische Mess-, Steu er-, Regel- und Laborgeräte - Teil 2-101: Besondere Anforderung en an In- vitro-Diagnostik (IVD) Medizingeräte (IEC 61010-2-1 01:2018, modifiziert); Deutsche Fa

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

IEC 61010-2-101; EN IEC 61010-2-101; CSA-C22.2 No. 61010-2-101; UL 61010-2-101; IEC 61010-2-091; EN IEC 61010-2-091; UL 61010-2-091; CSA C22.2 No. 61010-2-091; IEC 61010-2-040; EN IEC 61010-2-040; UL 61010-2-040; CSA C22.2 No. 610

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

IEC 61010-2-101; EN IEC 61010-2-101; CSA C22.2 No. 61010-2-101; UL 61010-2-101 Dentistry—Powered polymerization activators ISO 10650; EN ISO 10650 Wheelchair seating Part 10: Resistance to ignition of postural support devic

Intertek Testing Services NA
Kentwood, MI, US

IEC 61010-2-101; IEC 61010-2-201; UL 61010-1; CAN/CSA C22.2 No. 1010.1; CAN/CSA C22.2 No. 61010-1; AS/NZS 61010; UL 61010-2-010; CSA C22.2 No. 61010-2- 010; UL 61010-2-011; CSA C22.2 No. 61010-2-011; UL 61010-2-030; CSA C22.2 No. 61010

cetecom advanced
Saarbrücken, DE

IEC 61010-2-101:2023-12 Sicherheitsbestimmun gen für elektrische Mess-, Steuer-, Regel- und Laborgeräte - Teil 2-101: Besondere Anforderungen an In-

SGS Korea Co., Ltd. (Gunpo Laboratory)
Gunpo-si, KR

IEC 61010-2-101; EN IEC 61010-2-201; UL 61010-2-010; UL 61010-2-020; UL 61010-2-040; UL 61010-2-051; UL 61010-2-081; UL 61010-2-101; UL 61010-2-201; CAN/CSA C22.2 No. 61010-2-010; CAN/CSA C22.2 No. 61010-2-020; CAN/CSA C22.2 No. 61

TUV Rheinland (China)
Beijing, CN

IEC 61010-2-101:2018; EN 61010-2-101:2017 IEC 61010-1 Ed 3.1 2017-01 10.5.3 2) Vicat softening 11.7 Fluid pressure and leakage 12.2 Ionizing radiation 12.3 Ultraviolet (UV) radiation 12.4 Microwave radiation 12.5 Sound level and ult

Eurofins Electric & Electronics Finland
Oulu, FI

IEC 61010-2-101 Oulu, Elektroniikkatie Audio- ja videolaitteet sekä tieto- ja tietoliikennetekniikan laitteet Audio/video, information and communication technology equipment Turvallisuustestaus Safety FLX* IEC/EN/UL/CSAC 22.2/AS/NZ 62368-1:

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

IEC 61010-2-101; IEC 61010-2-101:2015; IEC 61010-2-101:2002; EN 61010-2-101; EN 61010-2-101:2017; EN 61010.2-101:2002; CAN/CSA C22.2 No. 61010-2- 101; CAN/CSA C22.2 No. 61010-2- 101:2015; CAN/CSA C22.2 No. 61010-2- 101:2004;

Nemko S.p.A. a socio unico
Biassono, IT

Nemko S.p.A. a socio unico Via del Carroccio, 4 20853 Biassono MB Allegato al certificato di accreditamento n. 00036 rev. 4 del 23/01/2025 UNI CEI EN ISO/IEC 17025:2018 Revisione: 35 Sede A Data: 15/10/2025 pag. 1 di 40 ELENCO

Bay Area Compliance
Sunnyvale, CA, US

IEC 61010-2-101 (2022/A11:2022); BS EN 62368-1 (2014); BS EN IEC 62368-1:2020/A11; CNS 15598-1; IEC 62087-1:2015; EN 62087-1:2016; IEC 62368-3:2017; AS NZS 62368.1-2018 LITE (excluding, Stress Corrosion, Rough Service Luminaires

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

Test Technology: Test Method(s): Product Safety (Cont’d) IEC/EN BS EN 60695-10-2; IEC/EN BS EN 60695-2-10; IEC/EN BS EN 60695-2-11; IEC/EN BS EN 60695-2-12; IEC/EN BS EN 60695-2-13; IEC/EN/BS EN 61010-2-101(excludin

Kiwa Primara
Kaufbeuren, DE

IEC 61010-2-101:2015); Deutsche Fassung EN 61010-2-101:2017 (in Verbindung mit DIN EN 61010-1 : 2011-07, solange eine gültige Akkreditierung hierfür besteht) DIN EN 61010-2-101 : 2003-09 ⊗ - Sicherheitsbestimmungen für elektrische Mes

TUV SUD Japan
Tokyo, JP

IEC 61010-2-101:2002; EN 61010-2-101:2002; IEC 61010-2-101:2015; EN 61010-2-101:2017; JIS C 61010-2-101:2017; IEC 61010-2-101:2018; CAN/CSA-C22.2 No. 61010-2-101:19 Measuring Equipment3 IEC 61010-1:2010 (Only secti

TUV Rheinland Italia
Pogliano Milanese, IT

IEC 61010-2-101:2022/A11:2022, IEC 61010-2-101:2018 _ EN 61010-2-101:2017, IEC 61010-2-101:2015, IEC 61010-2-101:2018 _ EN 61326-2-6:2013, EN IEC 61326-2-6:2021, IEC 61326-2-6:2012, IEC 61326-2-6:2020 _ Apparecchi elettrici per la cot

TUV SUD America
San Diego, CA, US

IEC 61010-2-101 (1Ed 2002, 2Ed 2015; 3Ed 2018); EN 61010-2-101 (2002, 2015, 2017); CAN/CSA-C22.2 No. 61010-2-101 (1Ed 2004, R:2009, R2014; 2Ed 2015; 3Ed 2019); UL 61010-2-101 (2Ed 2015; 3Ed 2019); EN IEC 61010-2-101:2022/A11:2022