IEC 60601-1-3 Accredited Testing Labs Worldwide
27 accredited laboratories in 9 countries hold IEC 60601-1-3 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle. In the register, IEC 60601-1-3 scope entries most often cover Combustible Gasses, Leakage Radiation, Radiation, Ionizing/Non-Ionizing in Medical equipment, electrical safety and EMC, Electrical equipment.
Available in 9 Countries
Top matrices for IEC 60601-1-3
Top analytes for IEC 60601-1-3
- Combustible Gasses (1)
- Leakage Radiation (1)
- Radiation, Ionizing/Non-Ionizing (1)
Sample labs
IEC 60601-1-3 2; 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; I
IEC 60601-1-3:2008 + A1:2013 + A2:2021); Deutsche Fassung EN 60601-1-3:2008 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2016 + A2:2021 DIN EN 60601-2-2 : 2018-12 Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für
IEC 60601-1-3; IEC 60601-1-3:2008; IEC 60601-1-3 Edition 2.1 2013-04; IEC 60601-1-3 Edition 2.2 2021-01 CONSOLIDATED VERSION; CSA C22.2 No. 60601-1-3; EN 60601-1-3 IEC 61010-1; IEC 61010-1 Edition 3.1 2017-01 CONSOLIDATED VERSION;
IEC 60601-1-3; IEC 60601-1-4; IEC 60601-1-8; IEC 60601-2-10; 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 60
IEC 60601-1-3; IEC 60601-1-3 Edition 2.2 2021-01 CONSOLIDATED VERSION; IEC 60601-1-4; 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 6060
IEC 60601-1-3:2008 + A1:2013 + A2:2021); Deutsche Fassung EN 60601-1-3:2008 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2016 + A2:2021 DIN EN 60601-1-3 : 2014-06 - Medizinische elektrische Geräte - Teil 1-3: Allgemeine Festlegungen für di
IEC 60601-1-3:2008/ A2:2021 EN 60601-1-3:2008 + A1:2013 EN 60601-1- 3:2008/A2:2021 DIN EN 60601-1-3:2014- 06 VDE 0750-1-3:2014-6 Medical electrical equipment - Part 1-3: General requirements for basic safety and essenDal performanc
IEC 60601-1-36; 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
IEC 60601-1-3 : 2008-01 Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral st andard: Radiation protection in diagnostic X-ray equipment + Amendment 1 : 2013-04 + Amendm
IEC 60601-1-3 Edition 2.2 2021-01 CONSOLIDATED VERSION; 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]; IE
IEC 60601-1-3:2008 + A1:2013 + A2:2021); Deutsche Fassung EN 60601-1-3:2008 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2016 + A2:2021 VDE 0750-1-3:2021-10 DIN EN 60601-1-3 : 2014-06 ⊗ - Medizinische elektrische Geräte - Teil 1-3:
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 60601-1-3; EN 60601-1-3; CAN/CSA C22.2 No. 60601-1-3 Medical device software -Software life cycle processes IEC 62304, EN 62304, ANSI/AAMI 62304, JIS T2304 Usability IEC 60601-1-6; EN 60601-1-6; CAN/CSA-C22.2 No. 60601-1
IEC 60601-1-3:2008 + A1:2013 + A2:2021); Deutsche Fassung EN 60601-1-3:2008 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2016 + A2:2021 DIN EN 60601-1-4 : 2001-04⊗ Medizinische elektrische Geräte - Teil 1-4: Allgemeine Festlegungen für
IEC 60601-1-3; EN 60601-1-3; CAN/CSA-C22.2 No. 60601-1-3; 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.
IEC 60601-1-3, EN 60601-1-3; CAN/CSA-C22.2 No. 60601-1-3 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance – Collateral standard: Usability IEC 60601-1-6, EN 60601-1-6; CAN/CSA
IEC 60601-1-3; EN 60601-1-3; DIN EN 60601-1-3; VDE 0750-1-3; IEC 60601-1-3 Edition 2.2 2021-01 CONSOLIDATED VERSION Medical electrical equipment − Part 1-6: General requirements for basic safety and essential performance − Col
IEC 60601-1-3; IEC 60601-1-3 Edition 2.2 2021-01 Consolidated Version; IEC 60601-1-4; 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 Versio
IEC 60601-1-3 (Radiation Protection in Diagnostic X-ray equipment); EN/IEC 60601-1-6 (Usability); EN/IEC 60601-1-8 (Alarms); EN/IEC 60601-1-11 (Home Healthcare); EN/IEC 60601-1-12 (Equipment for EMS use Environments); EN/IEC 60601-2-2
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
Test(s): Test Method(s) 1,2: Medical electrical equipment – Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment ISO 80601-2-69; EN ISO 80601-2-69; CAN/CSA-C22.2 No.80601-
IEC 60601-1-3 Edition 2.2 2021-01 CONSOLIDATED VERSION 12-336 IEC 60601-1-8 Edition 2.2 2020-07 CONSOLIDATED VERSION (excluding clauses listed in the “Exclusion” table above) 5-131 IEC 60601-2-43 Edition 2.2 2019-10 CONSOLIDATED VERSIO
IEC 60601-1-3:2008 + A1:2013 + A2:2021); German version EN 60601-1-3:2008 + Cor.:2010 + A1:2013 + A1:2013/AC:2014 + A11:2016 + A2:2021 DIN EN 60601-1-3 : 2014-06 ⊗ - Medical electrical equipment - Part 1-3: General requirements for bas
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 -1-1:2002 VDE 0750-1-1:2002 Medical el
IEC 60601-1-3 Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability IEC 60601-1-6 Medical electrical equipment - Part 1-8: General requirements for
IEC 60601-1-3:2008 +A1:2013+A2 :2021 EN 60601-1-3:2008 +A1:2013+A2 :2020 IP, S Programmable Electrical Medical Systems Electrical safety IEC 60601-1-4:1996 +A1 IP Medical electrical equipment Usability Elect
IEC 60601-1-3 Edition 2.2 2021-01 CONSOLIDATED VERSION 12-336 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