IEC 60601-2-63 Accredited Testing Labs Worldwide
25 accredited laboratories in 8 countries hold IEC 60601-2-63 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.
Available in 8 Countries
Top matrices for IEC 60601-2-63
Sample labs
IEC 60601-2-63 2; IEC 60601-2-65 2; EN 60601-1; EN 60601-1-3 2;
Leistungsmerkmale von Geräten zur Stimulation von Nerven und Muskeln (IEC 60601-2-10:2012 + A1:2016); Deutsche Fassung EN 60601-2-10:2015 + A1:2016 DIN EN 60601-2-18 : 2016-10 Medizinische elektrisch e Geräte - Teil 2-18: Besondere Fes
IEC 60601-2-63; IEC 60601-2-63 Edition 1.2 2021-05 CONSOLIDATED VERSION; IEC 62304; IEC 62366; IEC 62366-1; IEC 80601-2-60 Edition 2.0 2019-06; AAMI/CSA 60601-1 ED 3.2; CAN/CSA-C22.2 No. 60601-1:14; JIS T 0601-1 OFF, Office (e
Department Standard / in house procedure / Version Title of standard or in house procedure (deviaBons /reducBons modificaBons of standard) LocaBon/ reducBons VDE 0750 -2-50: 2022 Product Safety IEC 60601 -2-52:2009 + A1:
This document is a translation. The definitive version is the original German annex to the accreditation certificate. VDE 0750 -2-54:2010-05 + Ber. 1:2010 -07 + Ber. 2:2011 -12 + Ber. 3 : 2012-04 DIN EN 60601-2-57 : 2011-11 Medizinisc
IEC 60601-2-63 Edition 1.2 2021-05 CONSOLIDATED VERSION; IEC 60601-2-65 Edition 1.2 2021-05 CONSOLIDATED VERSION; IEC 80601-2-60 Edition 2.0 2019-06; ISO 80601-2-61 Second edition 2017-12 (Corrected version 2018- 02); ISO 80601-2-69 Sec
IEC 60601-2-63:2012 + A1:2017 + A2:2021); Deutsche Fassung EN 60601-2-63:2015 + A1:2019 + A2:2021 VDE 0750-2-63:2022-08 DIN EN 60601-2-65 : 2022-07 Medizinische elektrisch e Geräte - Teil 2-65: Besondere Festlegungen für die Sicherheit
IEC 60601-2-63 Edition 1.2 2021-05 CONSOLIDATED VERSION 12-339 IEC 60601-2-65 Edition 1.2 2021-05 CONSOLIDATED VERSION 12-340 ISO 80601-2-12 Second edition 2020-02 1-146 IEC 80601-2-30 Edition 2.0 2018-03 3-123 ANSI AAMI IEC 80601-2-30:
IEC 60601-2-63 Edition 1.2 2021-05 CONSOLIDATED VERSION (clause 202 only) 12-339 IEC 60601-2-65 Edition 1.2 2021-05 CONSOLIDATED VERSION (clause 202 only) 12-340 IEC 80601-2-77 Edition 1.0 2019-07 (clauses 201.17, 202 only) 6-438 I
IEC 60601-2-63; EN 60601-2-63; CSA C22.2 NO. 60601-2-63 Medical Electrical Equipment – Part 2-65: Particular Requirements for the Basic Safety and Essential Performance of Dental Intra-Oral X-Ray Equipment IEC 60601-2-65; EN 60601-
IEC 60601-2-63; EN 60601-2-63; CAN/CSA-C22.2 No. 60601-2-63
IEC 60601-2-63:2012 + A1:2017 + A2:2021); Deutsche Fassung EN 60601-2-63:2015 + A1:2019 + A2:2021 DIN EN 60601-2-64 : 2018-01 Medizinische elektrische Geräte - Teil 2-64: Besondere Festlegungen für die Sicherheit einschließlich der wese
IEC 60601-2-63; EN 60601-2-63; CAN/CSA-C22.2 No. 60601-2-63; IEC 60601-2-65; EN 60601-2-65; CAN/CSA-C22.2 No. 60601-2-65; EN 60601-1-9; CAN/CSA C22.2 No. 60601-1-9;
IEC 60601-2-63; EN 60601-2-63; CAN/CSA-C22.2 No. 60601-2-63 Medical electrical equipment – Part 2-65: Particular requirements for basic safety and essential performance of dental intra-oral X-ray equipment IEC 60601-2-65; EN 60601-
IEC 60601-2-63; EN 60601-2-63; DIN EN 60601-2-63; VDE 0750-2-63; IEC 60601-2-63 Edition 1.2 2021-05 CONSOLIDATED VERSION Medical electrical equipment − Part 2-65: Particular requirements for the basic safety and essential per
IEC 60601-2-63 (Ed. 1 + Am1 + Am2); IEC 60601-2-63 Edition 1.2 2021-05; IEC 60601-2-64 (Ed. 1); IEC 60601-2-64 Edition 1.0 2014-09; IEC 60601-2-66 (Ed. 1; Ed. 2; Ed. 3); IEC 60601-2-68 (Ed. 1; Ed. 2); IEC 60601-2-68 Edition 1.0 201
IEC 60601-2-63 : 2012-09 Medical electrical equipment - Part 2-63: Particular requirements for the basic safety and essential performance of dental extra-oral X-ray equipment + Amendment 1 : 2017-07 + Amendment 2 : 2021-05 IEC 60601-2-65 :
IEC 60601-2-63 (Dental Extra-oral X-ray Equipment); IEC 60601-2-65 Dental Intra-Oral X-Ray Equipment; EN/IEC 60601-2-68 (X-ray-based Image-guided Radiotherapy Equipment for use with Electron Accelerators, Light Ion Beam Therapy Equipment
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 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy IEC/EN IEC 60601-2-54; CAN/CSA-C22.2
(A2LA Certificate No. 0751.05) Revised 03/02/2026 Page 3 of 10 Test Technology: Test Method(s) 1, 2: EMC Medical (continued) IEC/EN 60601-2-25 (cl. 202 only); IEC/EN 60601-2-27 (cl. 202 only); IEC/EN 60601-2-31 (cl. 202 only); IEC/EN
IEC 60601-2-63 Edition 1.2 2021-05 CONSOLIDATED VERSION 12-339 IEC 60601-2-47 Edition 2.0 2012-02 (excluding clauses listed in the “Exclusion” table above) 3-155 IEC 80601-2-77 Edition 1.0 2019-07 6-438 3 This laboratory is only ac
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 -2-54:2016 VDE 0750-2-54:2016 Medica
IEC 60601-2-63 Medical electrical equipment - Part 2-65: Particular requirements for the basic safety and essential performance of dental intra- oral-X-ray equipment IEC 60601-2-65 Medical electrical equipment - Part 2-26: Particular
IEC 60601-2-63 Edition 1.2 2021-05 CONSOLIDATED VERSION 12-339 IEC 60601-2-65 Edition 1.2 2021-05 CONSOLIDATED VERSION 12-340 IEC 61010-1 Edition 3.1 2017-01 CONSOLIDATED VERSION; ANSI/UL 61010-1 3rd Ed, dated May 12, 2012 with revision