IEC 60601-2-10 Accredited Testing Labs Worldwide
44 accredited laboratories in 8 countries hold IEC 60601-2-10 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle. In the register, IEC 60601-2-10 scope entries most often cover Radiation, Ionizing/Non-Ionizing in Medical equipment, electrical safety and EMC.
Available in 8 Countries
Top matrices for IEC 60601-2-10
Top analytes for IEC 60601-2-10
- Radiation, Ionizing/Non-Ionizing (1)
Sample labs
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 60601-2-45 2; IEC 60601-2-54 2; IEC 60601-2-57; IEC 80601-2-60; IEC 60601-2-63 2; IEC 6
IEC 60601-2-10 : 2012-06 Medical electrical equipment - Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators + Amendment 1 : 2016-04 IEC 60601-2-18 : 2009-08 Medical electrica
Quellenverzeichnis Regelwerke/Prüfverfahren: DIN EN ISO 11197 : 2020-05 Medizinische Versorgungs einheiten (ISO 11197:2019); Deutsche Fassung EN ISO 11197:2019 DIN EN ISO 11197 : 2016-08 ⊗ - Medizinische Versorgungseinheiten (ISO 11197
IEC 60601-2-10; IEC 60601-2-10 Edition 2.1 2016-04; IEC 60601-2-10 Edition 2.2 2023-01 CONSOLIDATED VERSION; CSA C22.2 No. 60601-2-10; EN 60601-2-10 IEC 60601-2-34; IEC 60601-2-34 Edition 3.0 2011-05; IEC 60601-2-34:2024; CSA C22.
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 60601-2-36; IEC 60601-2-4; IEC 60601-2-40
IEC 60601-2-10:2012-06 Medical electrical equipment – Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators. + Amendment 1:2016-04 + Amendment 2:2023-01 IEC 60601-2-18:2009-08
IEC 60601-2-10:2012+AMD1:2016+AMD2:2023 CSV; IEC 60601-2-10; EN 60601-2-10; CAN/CSA-C22.2 No. 60601-2-10; IEC 60601-2-22; EN 60601-2-22; CAN/CSA-C22.2 No. 60601-2-22
IEC 60601-2-10:2012 + A1:2016); Deutsche Fassung EN 60601-2-10:2015 + A1:2016 DIN EN 60601-2-18 : 2016-10 Medizinische elektrische Geräte - Teil 2-18: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkma
Department Standard / in house procedure / Version Title of standard or in house procedure (deviaBons /reducBons modificaBons of standard) LocaBon/ reducBons Product Safety IEC 60601 -2-10:2012 + A1:2016 IEC 60601-2- 10:201
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
IEC 60601-2-10:2012); Deutsche Fassung EN 60601-2-10:2015 VDE 0750-2-10:2015-11⊗ DIN EN 60601-2-10 : 2003-04⊗ - Medizinische elektrische Geräte - Teil 2-10: Besondere Festlegungen für die Sicherheit von Geräten zur Stimulation von Nerv
IEC 60601-2-10 Edition 2.1 2016-04; ISO 80601-2-12 Second edition 2020-02; ISO 80601-2-12 Third edition 2023-11
IEC 60601-2-10:2012 + A1:2016); Deutsche Fassung EN 60601-2-10:2015 + A1:2016 VDE 0750-2-10:2017-09 DIN EN 60601-2-10 : 2015-11 ⊗ - Medizinische elektrische Geräte – Teil 2-10: Besondere Festlegungen für die Sicherheit einschließlich
IEC 60601-2-10 : 2012-06 Medical electrical equipment – Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators + Amendment 1 : 2016-04 + Amendment 2 : 2023-01 IEC 61010-2-101 :
Test Technology: Test Method(s) 2,3,4: Part 1-11: General requirements for basic safety and essential performance -- Collateral Standard: Requirements for medical electrical equipment and medical electrical equipment and medical ele
IEC 60601-2-10 Edition 2.1 2016-04 17-16 IEC 60601-2-18 Edition 3.0 2009-08 9-114 IEC 60601-2-22 Edition 3.1 2012-10 12-268 IEC 60601-2-25 Edition 2.0 2011-10 3-105
IEC 60601-2-10; EN 60601-2-10; BS EN 60601-2-10; CAN/CSA-C22.2 No. 60601-2-10; AS 60601.2.10; AAMI NS4 Endoscopic equipment IEC 60601-2-18; EN 60601-2-18; BS EN 60601-2-18; CAN/CSA C22.2 No. 60601-2-18; AS/NZS IEC 60601.2.18; J
IEC 60601-2-10:2012 + A1:2016); Deutsche Fassung EN 60601-2-10:2015 + A1:2016 VDE 0750-2-10: 2017-09 DIN EN 60601-2-10 : 2017-09 ⊗ - Medizinische elektrische Geräte - Teil 2-10: Besondere Festlegungen für die Sicherheit von Geräten z
IEC 60601-2-10 Edition 2.1 2016-04 (clause 202 only) 17-16 IEC 60601-2-16 Edition 5.0 2018-4 (clause 202 only) 9-121 IEC 60601-2-18: Edition 3.0 2009-08 (clause 202 only) 9-114 IEC 60601-2-19 Edition 3.0 2020-09 (clause 202 only) 6-461
IEC 60601-2-10; EN 60601-2-10; CSA-C22.2 NO. 60601-2-10 Medical Electrical Equipment - Part 2-18: Particular Requirements for the Basic Safety and Essential Performance of Endoscopic Equipment IEC 60601-2-18; EN 60601-2-18; CSA-C
IEC 60601-2-10; EN 60601-2-10 Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment IEC 60601-2-22; EN IEC 606
Test: Test Method(s) 1: Generic and Product Family Standards (cont.) IEC 62236-4; EN 50155; EN 55013; KN 13; EN 55020 (only for audio/video equipment without tuner); KN 20 (only for audio/video equipment without tuner); EN 50
IEC 60601-2-10; EN 60601-2-10; CAN/CSA-C22.2 No.60601-2-10 Endoscopic equipment IEC 60601-2-18; EN 60601-2-18; CAN/CSA-C22.2 No. 60601-2-18 Surgical, cosmetic, therapeutic and diagnostic laser equipment IEC 60601-2-22; EN IEC
IEC 60601-2-10:2012 + A1:2016); Deutsche Fassung EN 60601-2-10:2015 + A1:2016 DIN EN 60601-2-10 : 2015-11⊗ - Medizinische elektrische Geräte - Teil 2-10: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistun
IEC 60601-2-10 : 2012-06 Medical electrical equipme nt - Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators + Amendment 1 : 2016-04 + Amendment 2 : 2023-01 IEC 60601-2-10
IEC 60601-2-10:2012 + A1:2016); Deutsche Fassung EN 60601-2-10:2015 + A1:2016 DIN EN 60601-2-10 : 2003-04 ⊗ - Medizinische elektrische Geräte - Teil 2-10: Besondere Festlegungen für die Sicherh eit von Geräten zur Stimulation von Nerve
IEC 60601-2-10; EN 60601-2-10; CAN/CSA-C22.2 No.60601-2-10; ISO 80601-2-12; EN ISO 80601-2-12; CAN/CSA-C22.2 No. 80601-2-12; ISO 80601-2-13; EN ISO 80601-2-13; CAN/CSA-C22.2 No. 80601-2-13; IEC 80601-2-30; EN IEC 80601-2-30; AAM
IEC 60601-2-10; EN 60601-2-10; CAN/CSA-C22.2 No.60601-2-10A Medical electrical equipment – Part 2-18: Particular requirements for basic safety and essential performance of endoscopic equipment IEC 60601-2-18; EN 60601-2-18; CAN/CSA
IEC 60601-2-10; EN 60601-2-10; DIN EN 60601-2-10; VDE 0750-2-10; IEC 60601-2-10 Edition 2.1 2016-04
IEC 60601-2-10; IEC 60601-2-10 Edition 2.1 2016-04; IEC 60601-2-10 Edition 2.2 2023-01 Consolidated Version; IEC 60601-2-16; IEC 60601-2-16 Edition 5.0 2018-4; IEC 60601-2-18; IEC 60601-2-18 Edition 3.0 2009-08; IEC 60601-2-22; IEC 60
IEC 60601-2-10 Edition 2.1 2016-04 (Section(s) 201.17/202) 1; IEC 60601-2-11 Edition 3.0 2013-01 (Section(s) 201.17/202) 1; ANSI AAMI IEC 60601-2-16:2018 (Section(s) 201.17/202) 1; IEC 60601-2-18: Edition 3.0 2009-08 (Section(s) 201
IEC 60601-2-10:2012); Deutsche Fassung EN 60601-2-10:2015 VDE 0750-2-10:2015-110 Medizinische elektrische Geräte - Teil 2-18: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von endoskopischen Ger
IEC 60601-2-10 Edition 2.1 2016-04 17-16 IEC 60601-2-11 Edition 3.0 2013-01 12-255 IEC 60601-2-16 Edition 5.0 2018-4 9-121 ANSI AAMI IEC 60601-2-16:2018 9-121 IEC 60601-2-17 Edition 3.0 2013-11 12-272 IEC 60601-2-18 Edition 3.0 2009-08
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
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 60601-2-10 EMC Surgical devices and surgical aids Checking compliance with general and specific requirements - Endoscopy devices DIN EN 60601-2-18 IEC 60601-2-18
IEC 60601-2-10; Hemodialysis Equipment IEC 60601-2-16; Endoscopic Equipment IEC 60601-2-18;
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 -2-7:2000 VDE 0750-2-7:2000 Medical el
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
White Lab S.r.l. - Test'ing Via del Consorzio, 41 60015 Falconara Marittima AN Allegato al certificato di accreditamento n. 01044 rev. 7 del 21/05/2025 UNI CEI EN ISO/IEC 17025:2018 Revisione: 25 Sede A Data: 21/05/2025 pag. 4 d
IEC 60601-2-10:2012 + A1:2016); Deutsche Fassung EN 60601-2-10:2015 + A1:2016 DIN EN 60601-2-10 : 2015-11 ⊗ - Medizinische elektrische Geräte - Teil 2-10: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistu
IEC 60601-2-10 Edition 2.1 2016-04 17-16 ISO 80601-2-13 Second edition 2022-04; ISO 80601-2-13 First edition 2011-08-11 1-165 1-141 IEC 60601-2-16 Edition 5.0 2018-4; ANSI/AAMI IEC 60601-2-16:2018 9-121 IEC 60601-2-18 Edition 3.0 20
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 60601-2-10 Edition 2.1 2016-04 17-16 IEC 60601-2-18 Edition 3.0 2009-08 9-114 IEC 60601-2-19 Edition 3.0 2020-09 6-461 IEC 60601-2-20 Edition 3.0 2020-09 6-462 IEC 60601-2-21 Edition 3.0 2020-09 6-463 IEC 60601-2-22 Edition 3.1 201