IEC 60601-2-57 Accredited Testing Labs Worldwide
27 accredited laboratories in 6 countries hold IEC 60601-2-57 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.
Available in 6 Countries
Top matrices for IEC 60601-2-57
Sample labs
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 60601-2-57; IEC 60601-2-57 Edition 1.0 2011-01; IEC 60601-2-57 Edition 2.0 2023-07; CSA C22.2 No. 60601-2-57; EN 60601-2-57 IEC 60601-2-16; IEC 60601-2-16 Edition 5.0 2018-4; IEC 60601-2-16:2025; ANSI AAMI IEC 60601-2-16; ANS
IEC 60601-2-57; IEC 60601-2-5; IEC 60601-2-7; IEC 80601-2-69; UL 187; UL 60601-1 (excluding Clauses 36, 37, 40, 41, and 44.7) Miscellaneous Electrical Equipment CAN/CSA B149.3; CAN/CSA-C22.2 No. 102; CAN/CSA-C22.2 No. 103; C
IEC 60601-2-57 Edition 1.0 2011-01; IEC 60601-2-57; EN 60601-2-57; CAN/CSA-C22.2 No. 60601-2-57, (excluding 201.6.1.102, 201.10.103, 201.13.1.101); IEC 60601-2-62:2013; EN 60601-2-62:2015; CAN/CSA-C22.2 No. 60601-2-62:15, (excludi
IEC 60601-2-57:2011); Deutsche Fassung EN 60601-2-57:2011 Gültig ab: 27.08.2025 Ausstellungsdatum: 27.08.2025 Seite 27 von 38
Test Technology: Test Method(s)2,3: Medical Equipment (cont.) EN 60601-2-336 (Excluding Cl 201.17, 202); EN 60601-2-34 (Excluding Cl 201.17
IEC 60601-2-57:2011); Deutsche Fassung EN 60601-2-57:2011 VDE 0750-2-57:2011-11 DIN EN 60601-2-63 : 2022-08 Medizinische elektrische Geräte – Teil 2 -63: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistun
IEC 60601-2-57 Edition 1.0 2011-01; IEC 60601-2-57 Edition 2.0 2023-07; IEC 80601-2-58 Edition 3.0 2024-03; IEC 80601-2-58 Edition 2.0 2014-09; ANSI AAMI IEC 80601-2-58:2014; IEC 60601-2-62 Edition 1.0 2013-07; IEC 60601-2-63 Edition
IEC 60601-2-57:2011); Deutsche Fassung EN 60601-2-57:2011 VDE 0750-2-57:2011-11 DIN EN 60601-2-62 : 2016-04 Medizinische elektrisch e Geräte - Teil 2-62: Besondere Anforderungen an die Sicherheit einschließlich der wesentlichen Leistun
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 VERSION 12-340 ISO 80601-2-12 Second edit
Test Technology: Test Method(s) 2,3,4: Part 2-30: Particular requirements for the basic safety and essential performance of automated non- invasive sphygmomanometers IEC 80601-2-30; ANSI AAMI IEC 80601-2-30; CSA C22.2 NO.80601-2-
IEC 60601-2-57 Edition 1.0 2011-01 12-242 IEC 61010-1 Edition 3.1 2017-01 CONSOLIDATED VERSION 19-34 IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION 19-49 IEC 80601-2-30 Edition 2.0 2018-03 3-123 IEC 80601-2-60 Edition 2.0 2019-06
IEC 60601-2-57; EN 60601-2-57; BS EN 60601-2-57; CAN/CSA C22.2 No. 60601-2-57; AS IEC 60601.2.57
IEC 60601-2-57; EN 60601-2-57; CAN/CSA-C22.2 No. 60601-2-57
IEC 60601-2-57; EN 60601-2-57 Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipment IEC 60601-2-83; EN IEC 60601-2-83 Safety requirements
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; EN 60601-2-62; CAN/CSA-C22.2 No. 60601-2-62 Dental extra-oral X-ray equipment IEC 60601-2-63; EN
IEC 60601-2-57:2011); Deutsche Fassung EN 60601-2-57:2011 VDE 0750-2-57:2011-11 DIN EN 60601-2-62 : 2016-04 Medizinische elektrische Geräte - Teil 2-62: Besondere Anforderungen an die Sicherheit einschließlich der wesentlichen Leistung
IEC 60601-2-57: Edition 1.0 2011-01; IEC 61010-1: Edition 3.1 2017-01; IEC/ANSI/AAMI 60601-1-12; IEC/EN/UL 61010-2-030; CSA C22.2 No. 61010-2-030 Enclosure Integrity IEC 60529; IPX1 and IPX 2; IPX3 through IPX8 (water); IP1X th
IEC 60601-2-57:2023 Excluding: 201.6.1.102: risk group class 201.10.103: output uniformity 201.12: accuracy of controls EN 60601-2-57: 2011 E, F F Excluding: 201.6.1.102: risk group class 201.10.103: output
IEC 60601-2-57; EN 60601-2-57; CAN/CSA-C22.2 No. 60601-2-57; ISO 80601-2-61; EN ISO 80601-2-61; CAN/CSA-C22.2 No. 80601-2-61; ISO 80601-2-70; EN ISO 80601-2-70; CAN/CSA-C22.2 No.80601-2-70; ISO 80601-2-72; EN ISO 80601-2-
IEC 60601-2-57; EN 60601-2-57; CAN/CSA-C22.2 No. 60601-2-57 Medical electrical equipment – Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature scree
IEC 60601-2-57; IEC 60601-2-57 Edition 2.0 2023-07; IEC 60601-2-57 Edition 1.0 2011-01; IEC 80601-2-58; IEC 80601-2-60; IEC 80601-2-60 Edition 2.0 2019-06; ISO 80601-2-61; ISO 80601-2-61 Second edition 2017-12 (Corrected version
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 60601-2-68 (X-ray-based Image-guided Radiotherapy Equipment for use with
IEC 60601-2-57 Edition 1.0 2011-01 12-242 IEC 60601-2-57 Edition 2.0 2023-07 12-355 IEC 80601-2-59 Edition 2.0 2017-09 6-405 IEC 80601-2-60 Edition 2.0 2019-06 4-262 ISO 80601-2-61 Second Edition 2017-12 (Corrected Version 2018-02) 1-13
IEC 60601-2-57 - Home light therapy devices DIN EN IEC 60601-2-83 - Devices for photodynamic therapy and photodynamic diagnostic devices IEC 60601-2-75 - Microwave therapy devices DIN EN 60601-2-6 IEC 60601-2-6 - Infant
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
IEC 60601-2-57 Edition 2.0 2023-07; IEC 60601-2-57 Edition 1.0 2011-01 12-355 12-242 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