IEC 60601-1-6 Accredited Testing Labs Worldwide
37 accredited laboratories in 11 countries hold IEC 60601-1-6 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation. In the register, IEC 60601-1-6 scope entries most often cover Combustible Gasses in Medical equipment, electrical safety and EMC, Electrical equipment.
Available in 11 Countries
Top matrices for IEC 60601-1-6
Top analytes for IEC 60601-1-6
- Combustible Gasses (1)
Sample labs
IEC 60601-1-6; IEC 62366-1; IEC 60601-1-8; IEC TR 62366-2; IEC 60601-1-11; IEC 60601-2-2; IEC 60601-2-10; 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 60601-1-6; IEC 60601-1-6 Edition 3.1 2013-10; IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION; CSA C22.2 No. 60601-1-6; EN 60601-1-6 IEC 60601-1-8; IEC 60601-1-8:2006; IEC 60601-1-8 Edition 2.1 2012-11; IEC 60601-1-8 Edi
IEC 60601-1-6; IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION; IEC 60601-2-5; IEC 60601-2-5: Edition 3.0 2009-07; 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 60601-2-2
IEC 60601-1-6; EN 60601-1-6; CAN/CSA-C22.2 No. 60601-1-6; IEC 62366-1; EN 62366-1; CAN/CSA-IEC 62366-1; ANSI/AAMI/IEC 62366-1; IEC 60601-1-8; EN 60601-1-8; ANSI/AAMI/IEC 60601-1-8; CAN/CSA-C22.2 No. 60601-1-8; IEC 60601-1-11; EN 606
Department Standard / in house procedure / Version Title of standard or in house procedure (deviaBons /reducBons modificaBons of standard) LocaBon/ reducBons Product Safety IEC 60598 -2-20:2014 EN 60598-2-20:2015 DIN EN 60
IEC 60601-1-6; IEC 60601-1-8; IEC 60601-1-10; IEC 60601-1-11 (Excluding Cl 4.2, 8.3, 10.1, 12); IEC 60601-1-12 (Excluding Cl 6.2, 8.1, 10.1, 12); IEC 60601-2-16 (Excluding Cl 201.17); IEC 60601-2-2 (Excluding Cl 201.17, 202); IEC 6
IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION; IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021]; IEC 60601-1-10 Edition 1.2 2020-07 CONSOLIDATED VERSION; I
Tests: Standard(s) 2: Laboratory / Process Control / Test Equipment Products (excluding UV Radiation, Flammable Liquids, Cathode ray tubes test) (continued) UL 61010-2-040:2021, Ed. 3; UL 61010-2-051:2015, Ed. 3; UL 61010-2-051:
IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION 5-132 IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION 5-131 IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED VERSION 19-38 IEC 60601-2-2 Edition 6.0 2017-03 6-389 IEC 60601-2-
Test Technology: Test Method(s) 2,3,4: General Efficiency Test Uniform Test Method for Measuring the Energy Consumption of Battery Chargers Appendix Y to Subpart B, 10 CFR Part 430 – ENERGY CONSERVATION PROGRAM FOR CONSUM
IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION 5-132 IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION 5-131 IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED VERSION 19-38 IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSI
IEC 60601-1-6; EN 60601-1-6; BS EN 60601-1-6; CAN/CSA-C22.2 No 60601-1-6; AS IEC 60601.1.6; JIS T 60601-1-6 Alarm systems in medical electrical equipment and medical electrical systems IEC 60601-1-8; EN 60601-1-8; BS EN 60601
IEC 60601-1-6; EN 60601-1-6; EXCLUDED MEASUREMENTS: - Not accredited for RISK ASSESSMENT 3 - Defibrillation protection - Pressure vessels - X-radiation - Microwave radiation - Lasers - Sterilization - Lithium batteries per IEC 600
IEC 60601-1-6; EN 60601-1-6; CAN/CSA-C22.2 NO. 60601-1-6 Medical Electrical Equipment - Part 1-8: General Requirements for Basic Safety and Essential Performance - Collateral Standard: General Requirements, Tests and Guidance for Al
IEC 60601-1-6; EN 60601-1-6 Medical devices – Part 1: Application of usability engineering to medical device IEC 62366-1; EN 62366-1; ANSI AAMI IEC 62366-1 1 When the date, edition, version, etc. is not identified in the scope o
IEC 60601-1-6; EN 60601-1-6; CAN/CSA-C22.2 No. 60601-1-6; IEC 62366; EN 62366; ANSI/AAMI/IEC 62366; CAN/CSA-IEC 62366; IEC 62366-1; EN 62366- 1; CAN/CSA-IEC 62366-1; ANSI/AAMI/IEC 62366-1 Environmentally conscious design IEC 60601-1
IEC 60601-1-6:2010 + AMD1:2013 (incl IEC 62366-1:2007 + AMD1:2014) IEC 60601-1-6:2010 + AMD1:2013 + AMD2:2020 EN 60601-1-6:2010 +A1:2015 + A2:2021 (incl IEC 62366-1:2015 + AMD1:2020) F Alarm systems in medical Electrica
IEC 60601-1-6: 2010 +A1: 2013 +A2: 2020 C, G SAFETY TESTS2 EN 60601-1-6: 2010 +A1: 2015 +A2: 2021 Medical Electrical Equipment (incl IEC 62366-1: 2015 + A1:2020) (incl EN 62366-1: 2015 +A1: 2020) Nerve and muscle stimula
IEC 60601-1-6; EN 60601-1-6; CAN/CSA-C22.2 No. 60601-1-6; IEC 62366; EN 62366; ANSI/AAMI/IEC 62366; CAN/CSA-IEC 62366; IEC 62366-1; EN 62366-1; CAN/CSA-IEC 62366-1; ANSI/AAMI/IEC 62366-1; IEC 60601-1-8; EN 60601-1-8; ANSI/AAM
IEC 60601-1-6, EN 60601-1-6; CAN/CSA-C22.2 No. 60601-1-6 Medical devices - Application of usability engineering to medical devices IEC 62366; EN 62366; IEC 62366-1; EN 62366-1; CSA IEC 62366-1; ANSI/AAMI/IEC 62366-1 Medical ele
IEC 60601-1-6; EN 60601-1-6; DIN EN 60601-1-6; VDE 0750-1-6; IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION
IEC 60601-1-6; IEC 60601-1-6 Edition 3.2 2020-07 Consolidated Version; IEC 60601-1-8; IEC 60601-1-8 Edition 2.2 2020-07 Consolidated Version; IEC 60601-1-10; IEC 60601-1-10 Edition 1.2 2020-07 Consolidated Version;
IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION 5-132 IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION 5-131 ANSI AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021] 5-131 IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDAT
Test Technology: Test Method(s) 1, 4: Product Safety Measurement Equipment2, 3 IEC/EN/KS C IEC/UL 61010-1; CAN/CSA C22.2 No. 61010-1; IEC/EN 61010-2-010; IEC/EN 61010-2-020; IEC/EN 61010-2-040; IEC/EN 61010-2-051; IEC/EN 61010-2-08
IEC 60601-1-6;EN 60601-1-6; CAN/CSA-C22.2 No. 60601-1-6
The testing laboratory is permitted, without being required to inform and obtain prior approval from DAkkS, to use standards or equivalent testing methods listed here with different issue dates. The testing laboratory maintains a current
IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION 5-132 IEC 60601-2-2 Edition 6.0 2017-03 (excluding clauses listed in the “Exclusion” table above) 6-389 IEC 60601-2-18: Edition 3.0 2009-08 9-114 IEC 60601-2-22 Edition 4.0 2019-
Przedmiot badań/wyrób Rodzaj działalności/badane cechy/metoda Dokumenty odniesienia Medyczne urządzenia elektryczne Szczeliny w ochronie przed zagrożeniami mechanicznymi Zakres: (0,1 - 1000) mm Metoda: pomiar wielkości liniowych PN
IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION; CSA CAN/CSA-C22.2 No. 60601-1-6:11 - Medical electrical equipment — Part 1-6: Edition 3.2; IEC 62366-1:2020 1.1 Edition; IEC 62304:2015 1.1 Edition; IEC 60601-1-12 Edition 1.1 202
IEC 60601-1-6; IEC 60601-1-6:2010 + A1:2013 + A2:20201; CAN/CSA C22.2 No. 60601-1-6; EN 60601-1-6; NBR IEC 60601-1-6;
IEC 60601-1-6 Edition 3.2 2020-07 Infant Incubators Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators IEC 60601-2-19 Edition 3.0 2020-09 Medical
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
IEC 60601-1-6 Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment a
IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION 5-132 IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION; ANSI/AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021] 5-131 IEC 60601-2-10 Edition 2.1 2016-04 17-16 ISO 80
IEC 60601-1-6:2004; IEC 60601-1-6:2010; IEC 60601-1-6:2010 + A1:2013; EN 60601-1-6:2010; EN 60601-1-6:2010/A1:2015; IEC 60601-1-8:2003 + A1:2006; IEC 60601-1-8:2006; IEC 60601-1-8:2006 + A1:2012 + A2:2020; EN 60601-1-8:2007 + A1
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
IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION 5-132 IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION 5-131 ANSI AAMI IEC 60601-1-8:2006 and A1:2012 [Including AMD 2:2021] 5-131 IEC 60601-1-10 Edition 1.2 2020-07 CONSOLID