IEC 60601-2-83 Accredited Testing Labs Worldwide
14 accredited laboratories in 6 countries hold IEC 60601-2-83 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation.
Available in 6 Countries
Top matrices for IEC 60601-2-83
Sample labs
IEC 60601-2-83; IEC/EN 60601-1-11; IEC/EN 61326-1; IEC/EN 61326-2-1; IEC/EN 61326-2-2; IEC/EN 61326-2-3; IEC/EN 61326-2-4; IEC/EN 61326-2-5; IEC/EN 61326-2-6; EN 50130-4; KS C 9811; EN 55011; CISPR 11; AS CISPR 11; KS C 9814-1; IEC/EN
IEC 60601-2-83; EN 60601-2-83; CAN/CSA-C22.2 No. 60601-2-83, (excluding 201.6.101, 201.10.107); IEC 80601-2-30; EN 80601-2-30; ANSI/AAMI/IEC 80601-2-30 (excluding 201.15.3.5); IEC 80601-2-60; EN 80601-2-60; CAN/CSA-C22.2 No. 806
IEC 60601-2-83 (Excluding Cl 201.6, 201.10, 201.17, 202) ISO 80601-2-12 (Excluding Cl 201.17, 202); ISO 80601-2-13 (Excluding Cl 201.17); IEC 80601-2-26 (Excluding Cl 201.17, 202); IEC 80601-2-30 (Excluding Cl 201.17, 202); IEC 80601-2
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 60601-2-83; EN IEC 60601-2-83; CSA C22.2 No. 60601-2-83
IEC 60601-2-83; EN IEC 60601-2-83 Safety requirements for electrical equipments for measurement, control and laboratory use - Part 1: General requirements IEC 61010-1; EN 61010-1; ANSI UL 61010-1 Safety standards for electrical
IEC 60601-2-83; EN 60601-2-83; CAN/CSA-C22.2 No. 60601-2-83 Electroencephalographs IEC 80601-2-30; EN IEC 80601-2-30; AAMI/IEC 80601-2-30; CSA C22.2 NO. 80601-2-30 Automated non-invasive sphygmomanometers IEC 80601-2-49; EN IE
IEC 60601-2-83 : 2021-05 Medizinische elektrische Geräte - Teil 2-83: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Heim-Lichttherapiegeräten (IEC 60601-2- 83:2019); Deutsche Fassung EN IE
IEC 60601-2-83:2019 + Amd1:2022 Excluding: 201.6.101: risk group classification 201.10.103 c stray optical radiation 201.107 optical radiation at a sampling frequency (flickering and flashing light) IEC 60601-2-83:2019 E, F
IEC 60601-2-83; EN IEC 60601-2-83; ISO 80601-2-84; ISO 11195; ASTM E 1112; ASTM E 1965; IEC 60601-1-3; EN 60601-1-3; CAN/CSA-C22.2 No. 60601-1-3; IEC 60601-2-18; EN 60601-2-18; CAN/CSA-C22.2 No. 60601-2-18; IEC 60601-2-28
IEC 60601-2-83; EN IEC 60601-2-83 Medical suction equipment – Part 1: Electrically powered suction equipment ISO 10079-1; EN ISO 10079-1; CAN/CSA-ISO 10079-1 Medical Suction Equipment – Part 3: Suction equipment powered from a vacu
IEC 60601-2-83; IEC 60601-2-83:2019; IEC 60601-2-83:2019+AMD1:2022 Laboratory Equipment (excluding Vicat Softening and CRT/High Vacuum) IEC 61010-1 (Ed 3, Ed 3.1)3; IEC 61010-1 Edition 3.1 2017-01 (Excluding Clause 10.5.3 Vica
IEC 60601-2-83 (Home Light Therapy Equipment); EN/IEC 80601-2-30 (Automated Non-Invasive BP)
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 phototherapy devices DIN EN 60601-2-50 IEC 60601-2