IEC 60601-1-10 Accredited Testing Labs Worldwide
15 accredited laboratories in 4 countries hold IEC 60601-1-10 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.
Available in 4 Countries
Top matrices for IEC 60601-1-10
Sample labs
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
This document is a translation. The definitive version is the original German annex to the accreditation certificate. Geräten und in medizinischen elektrischen Systemen (IEC 60601-1- 8:2006 + A1:2012); Deutsche Fassung EN 60601 -1-8:2007
IEC 60601-1-10 Edition 1.2 2020-07 CONSOLIDATED VERSION; IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED VERSION; ANSI AAMI HA60601-1-11:2015 [Including AMD1:2021]; IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC
IEC 60601-1-10:2007 + A1:2013); Deutsche Fassung EN 60601- 1-10:2008 + A1:2015 DIN EN 60601-1-10 : 2008-11 ⊗ - Medizinische elektrische Geräte - Teil 1-10: Allgemeine Festlegungen für die Sicherheit einschließlich der wesentlichen Leist
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 60601-1-10:2007 + A1:2013 + A2:2020); Deutsche Fassung EN 60601-1-10:2008 + A1:2015 + A2:2021 DIN EN 60601-1-10 : 2016-040 - Medizinische elektrische Geräte - Teil 1-10: Allgemeine Festlegungen für die Sicherheit einschließlich der
10:2007 + A1:2013); German version EN 60601 -1-10:2008 + A1:2015 DIN EN 60601-1-11 : 2021-12 Medical electrical equi pment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements
IEC 60601-1-10; EN 60601-1-10; CAN/CSA-C22.2 No. 60601-1-10; IEC 60601-2-2; EN IEC 60601-2-2; ANSI/AAMI 60601-2-2; CSA C22.2 NO. 60601-2-2; IEC 60601-2-4; EN 60601-2-4; ANSI/AAMI 60601-2-4; CAN/CSA-C22.2 NO. 60601-2-4; IEC 6
IEC 60601-1-10; EN 60601-1-10; CSA C22.2 NO. 60601-1-10 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance – Collateral standard: Requirements for medical electrical equipment and med
IEC 60601-1-10; EN 60601-1-10; DIN EN 60601-1-10; VDE 0750-1-10; IEC 60601-1-10 Edition 1.2 2020-07 CONSOLIDATED VERSION Medical electrical equipment − Part 1-11: General requirements for basic safety and essential performance −
IEC 60601-1-10; IEC 60601-1-10 Edition 1.2 2020-07 Consolidated Version;
according DIN EN ISO/IEC 17025:2018 Valid from : 03 .05.2024 Date of issue : 09.05.2025 Page 24 of 42 This document is a translation. The definitive version is the original German annex to the accreditation certificate. DIN
IEC 60601-1-10; IEC 60601-1-10:2007 + A1:2013 + A2:20201; CAN/CSA C22.2 No. 60601-1- 10; EN 60601-1-10; Medical Electrical Equipment and Medical Electrical Systems used in the Home Healthcare Environment IEC 60601-1-11; IEC 60
IEC 60601-1-10 Edition 1.2 2020-07 CONSOLIDATED VERSION 19-37 IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED VERSION; ANSI/AAMI HA60601-1-11:2015 [Including AMD1:2021] 19-38 19-47 IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSIO
IEC 60601-1-10 Edition 1.2 2020-07 CONSOLIDATED VERSION 19-37 IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED VERSION 19-38 IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION 19-39 IEC 60601-2-10 Edition 2.1 2016-04 17-16 IEC 60601