IEC 60601-2-54 Accredited Testing Labs Worldwide
25 accredited laboratories in 7 countries hold IEC 60601-2-54 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.
Available in 7 Countries
Top matrices for IEC 60601-2-54
Sample labs
IEC 60601-2-54 2; IEC 60601-2-57; IEC 80601-2-60; IEC 60601-2-63 2; IEC 60601-2-65 2; EN 60601-1; EN 60601-1-3 2;
IEC 60601-2-54:2009 + Cor.:2010 + Cor.:2011 + A1:2015 + A2:2018); Deutsche Fassung EN 60601-2-54:2009 + A1:2015 + A2:2019 DIN EN 60601-2-63 : 2022-08 Medizinische elektrisch e Geräte - Teil 2-63: Besondere Festlegungen für die Sicherhei
IEC 60601-2-54 Edition 2.0 2022-09; ISO 80601-2-55 Second edition 2018-02; ISO 80601-2-55 Second edition 2018-02 [Including AMD1:2023]; IEC 80601-2-60 Edition 2.0 2019-06; ISO 80601-2-61 Second edition 2017-12 (Corrected version 2018-02
IEC 60601-2-54 (Ed 1.1, Ed 1.2); IEC 60601-2-54 Edition 2.0 2022-09; 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
IEC 60601-2-54:2009 + Cor.:2010 + Cor.:2011 + A1:2015 + A2:2018); Deutsche Fassung EN 60601-2-54:2009 + A1:2015 + A2:2019 DIN EN 60601-2-54 : 2016-070 - Medizinische elektrische Geräte — Teil 2-54: Besondere Festlegungen für die Sicherheit
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:
IEC 60601-2-54:2009 + Cor.:2010 + Cor.:2011 + A1:2015); Deutsche Fas sung EN 60601 -2-54:2009 + A1:2015 VDE 0750-2-54:2016-07 DIN EN 60601-2-54 : 2010-05⊗ - Medizinische elektrische Geräte - Teil 2 -54: Besondere Festlegungen für die S
IEC 60601-2-54 Edition 2.0 2022-09; ISO 80601-2-55 Second edition 2018-02; ISO 80601-2-55 Second edition 2018-02 [Including AMD1:2023]; ISO 80601-2-56 Second edition 2017-03; IEC 60601-2-57 Edition 1.0 2011-01; IEC 60601-2-57 Edition 2
IEC 60601-2-54:2009 + Cor.:2010 + Cor.:2011 + A1:2015 + A2:2018); Deutsche Fassung EN 60601-2-54:2009 + A1:2015 + A2:2019 VDE 0750-2-54:2020-03 DIN EN 60601-2-54 : 2016-07 ⊗ - Medizinische elektrische Geräte – Teil 2-54: Besondere Fe
IEC 60601-2-54 Edition 2.0 2022-09 12-348 IEC 60601-2-57 Edition 1.0 2011-01 12-242 IEC 60601-2-57 Edition 2.0 2023-07 12-355 IEC 60601-2-63 Edition 1.2 2021-05 CONSOLIDATED VERSION 12-339 IEC 60601-2-65 Edition 1.2 2021-05 CONSOLIDATED
IEC 60601-2-54 (clause 202 only); IEC 60601-2-62 (clauses 201.17, 202 only); IEC 60601-2-63 (clause 202 only); IEC 60601-2-65 (clause 202 only); IEC 80601-2-77 (clauses 201.17, 202 only); IEC/TR 60601-4-2 Edition 1.0 2016-05; IEC TS 60
IEC 60601-2-54; EN 60601-2-54; EN IEC 60601-2-54; CSA C22.2 NO. 60601-2-54 Medical Electrical Equipment – Part 2-63: Particular Requirements for the Basic Safety and Essential Performance of Dental Extra-Oral X- Ray Equipment IEC
IEC 60601-2-54; EN 60601-2-54; CAN/CSA-C22.2 No. 60601-2-54 Non-laser light source equipment IEC 60601-2-57; EN 60601-2-57; CAN/CSA-C22.2 No. 60601-2-57 High intensity therapeutic ultrasound (HITU) equipment IEC 60601-2-62;
IEC 60601-2-54:2009); Deutsche Fassung EN 60601-2-54:2009 + Berichtigung 1 : 2010-07 + Berichtigung 2 : 2011-12 + Berichtigung 3 : 2012-04 VDE 0750-2-54:2010-05 + Ber. 1:2010-07 + Ber. 2:2011-12 + Ber. 3:2012-04 DIN EN 60601-2-57 : 2
IEC 60601-2-54; EN 60601-2-54; CAN/CSA-C22.2 No. 60601-2-54; 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 60601-2-54; EN 60601-2-54; CAN/CSA-C22.2 No. 60601-2-54 Medical electrical equipment - Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors ISO 80601-2-55; EN ISO 80601-2-
IEC 60601-2-54; EN 60601-2-54; DIN EN 60601-2-54; VDE 0750-2-54; IEC 60601-2-54 Edition 2.0 2022-09 Medical electrical equipment − Part 2-55: Particular requirements for the basic safety and essential performance of respiratory
IEC 60601-2-54 (Ed. 1 + Am1 + Am2; Ed. 2); IEC 60601-2-54 Edition 2.0 2022-09; 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
IEC 60601-2-54 (X-ray Equipment or Radiography and Radioscopy); IEC 60601-2-57 (Non-Laser Light Source Equipment); EN/IEC 60601-2-63 (Dental Extra-oral X-ray Equipment); IEC 60601-2-65 Dental Intra-Oral X-Ray Equipment; EN/IEC 60601-2-6
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 60601-2-54; CAN/CSA-C22.2 No. 60601-2-54 Medical electrical equipment – Part 2-63: Particular requirements for the basic safety and essential performance of dental extra-oral X-ray equipment IEC/EN 60601-2-63; CSA C22.2 No. 6
(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 60601-2-54 Edition 2.0 2022-09 (excluding clauses listed in the “Exclusion” table above) 12-348 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 “Ex
IEC 60601-2-54:2009 + Cor.:2010 + Cor.:2011 + A1:2015); German version EN 60601-2-54:2009 + A1:2015 DIN EN 60601-2-54 : 2010-05 ⊗ - Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and essential per
IEC 60601-2-54:2009 + Cor.:2010 + Cor.:2011 + A1:2015); German version EN 60601-2-54:2009 + A1:2015 Medical Equipment ISO 80601 -2-56:2017 +A1:2018 Medical electrical equipment - Part 2 -56: Particular requirements for basic s