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.
Available in 11 Countries
Top matrices for IEC 61010-2-101
Top analytes for IEC 61010-2-101
- Blood-Glucose (1)
Sample labs
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
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 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
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
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
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
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
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
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
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
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-
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
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
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
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
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
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
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
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
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
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
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
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
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
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-
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
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
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
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
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
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
IEC 61010-2-101:2023-12 Sicherheitsbestimmun gen für elektrische Mess-, Steuer-, Regel- und Laborgeräte - Teil 2-101: Besondere Anforderungen an In-
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
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
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:
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 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
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
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
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
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
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
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