IEC 60601-2-2 Accredited Testing Labs Worldwide
45 accredited laboratories in 7 countries hold IEC 60601-2-2 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle. In the register, IEC 60601-2-2 scope entries most often cover Radiation, Ionizing/Non-Ionizing in Medical equipment, electrical safety and EMC, Electrical equipment.
Available in 7 Countries
Top matrices for IEC 60601-2-2
Top analytes for IEC 60601-2-2
- Radiation, Ionizing/Non-Ionizing (1)
Sample labs
IEC 60601-2-2 EN 60601-2-2 CSA C22.2 NO. 60601-2-2 201.15.101.5 NE thermal performance IEC 61010-1 EN 61010-1 ANSI UL 61010-1 CAN/CSA-C22.2 No. 61010-1 7.6 Wall mounting 10.5.3 Vicat softening test 11.6 IPX9 12.5.2 Ultrasonic p
IEC 60601-2-2 : 2017-03 Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories IEC 60601-2-2 : 2009-02⊗
IEC 60601-2-2:2018 DIN EN 60601-2-2 : 2010-01 ⊗ - Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hochfrequenz- Chirurgiegeräten und HF-chirurgis
IEC 60601-2-2; IEC 60601-2-2 Edition 6.0 2017-03; IEC 60601-2-2:2017/A1:2023; ANSI AAMI IEC 60601-2-2; ANSI AAMI IEC 60601-2-2:2017; CSA C22.2 No. 60601-2-2; EN IEC 60601-2-2 IEC 80601-2-60; IEC 80601-2-60 Edition 2.0 2019-06; CS
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 60601-2-2:2018-12 Medizinische elektrische Geräte – Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hochfrequenz-Chirurgiegeräten (IEC 60601-2-2:2017); Deutsche Fassung EN IEC
IEC 60601-2-2:2018-12 DIN EN 60601-2-3 : 2016-02 DIN EN 60601-2-4 : 2021-09 DAkkS Deutsche Akkreditierungsstelle in häuslicher Umgebung (IEC 60601-1-11:2015); Deutsche Fassung EN 60601-1-11:2015 DIN EN 60601-1-11 : 2011-030 - Medizinische e
Department Standard / in house procedure / Version Title of standard or in house procedure (deviaBons /reducBons modificaBons of standard) LocaBon/ reducBons Product Safety IEC 60601 -1-11:2015 IEC 60601-1- 11:2015/A1:2020
IEC 60601-2-2 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-4 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-16 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-19 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-20 (Cl 201.17, 202); ANSI/AAMI/IEC 60601-2-21 (Cl 201
IEC 60601-2-2 : 2018-12 Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hochfrequenz -Chirurgiegeräten (IEC 60601-2-2:2017); Deutsche Fassung EN
IEC 60601-2-2; IEC 60601-2-2 Edition 6.0 2017-03 1; IEC/EN 60244-4; EN 60255-5; IEC/EN 60255-2-26; IEC/EN 60529; EN 60601-2-22; IEC 60601-2-22; IEC 60601-2-22 Edition 3.1 2012-10 1; IEC/EN 61326-3-1; EN 16361; ISO 13849-1; ISO 13849
IEC 60601-2-2:2018 VDE 0750-2-2:2018-12 DIN EN 60601-2-2 : 2010-01 Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hochfrequenz- Chirurgiegeräte
IEC 60601-2-2:2017; ANSI AAMI IEC 80601-2-30: 2009&A1:2013 (R2016); ANSI AAMI IEC 80601-2-30:2018; ANSI AAMI IEC80601-2-35:2009/A1:2016; ANSI AAMI IEC 60601-2-47:2012/(R) 2016; CAN/CSA C22.2 No. 601.1; CSA C22.2.60601.1; EN 45502-1 (
IEC 60601-2-2 Edition 6.0 2017-03 6-389 IEC 60601-2-64:2014-09 12-318 IEC 60601-2-68 Edition 1.0 2014-09 12-319 IEC 61010-1 Edition 3.1 2017-01 CONSOLIDATED VERSION 19-34 1 The laboratory is only accredited for testing activities o
IEC 60601-2-25 Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment [Including: Corrigendum 1 (2012)] IEC/EN 60601-2-27; ANSI AAMI IEC 60601-2-27 Part 2-2: P
IEC 60601-2-2 Edition 6.0 2017-03 6-389 IEC 60601-2-22 Edition 3.1 2012-10 12-268 2 These methods have been assessed by A2LA according to A2LA’s FDA ASCA Program requirements. Accreditation by A2LA does not imply FDA ASCA-Accreditation
IEC 60601-2-2 Edition 6.0 2017-03 6-389 IEC 60601-2-5 Edition 3.0 2009-07 12-205 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 2
IEC 60601-2-2; EN IEC 60601-2-2; BS EN IEC 60601-2-2; CAN/CSA C22.2 No. 60601-2-2; AS/NZS IEC 60601.2.2; JIS T 0601-2-2; ANSI AAMI IEC 60601-2-2 Short-wave therapy equipment IEC 60601-2-3; EN 60601-2-3; BS EN 60601-2-3; CAN/CSA
IEC 60601-2-2 Edition 6.0 2017-03 (clauses 201.17, 202.7, 202.8 only) 6-389 IEC 60601-2-5: Edition 3.0 2009-07 (clause 201.17 only) 12-205 IEC 60601-2-6 Edition 2.1 2016-04 (clause 202 only) 6-423 IEC 60601-2-10 Edition 2.1 2016-04 (clau
IEC 60601-2-2; EN IEC 60601-2-2; ANSI AAMI IEC 60601-2-2; CSA C22.2 NO. 60601-2-2 Medical Electrical Equipment - Part 2-26: Particular Requirements for the Basic Safety and Essential Performance of Electroencephalographs IEC 80601-
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 60601-2-2; EN IEC 60601-2-2; ANSI/AAMI 60601- 2-2; CSA C22.2 NO. 60601-2-2
IEC 60601-2-2 : 2018-12 Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hochfrequenz-Chirurgiegeräten (IEC 60601-2-2:2017); Deutsche Fassung EN
IEC 60601-2-2, -3, -18, -20, -21, -22, -24, -25, -26, -27, -30, -32, -34, -35, -38, -39, -40, -41, -46; IEC/EN 61326-1 3; 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
IEC 60601-2-2 : 2018-12 Medical electrical e quipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories (IEC 60601-2-2:2017); G
IEC 60601-2-22:2019) ; Deutsche Fassung EN IEC 60601-2-22:2020 DIN EN 60601-2-26 : 2004-01 ⊗ Medizinische elektrische Geräte - Teil 2-26: Beson dere Festlegungen für die Sicherheit von Elektroenzephal ographen (IEC 60601-2-26:2002); De
IEC 60601-2-2; EN IEC 60601-2-2; ANSI/AAMI 60601-2-2; CSA C22.2 NO. 60601-2-2; IEC 60601-2-4; EN 60601-2-4; ANSI/AAMI 60601-2-4; CAN/CSA-C22.2 NO. 60601-2-4; IEC 60601-2-5; EN 60601-2-5; CAN/CSA-C22.2 No. 60601-2-5; IEC 6060
IEC 60601-2-2, EN IEC 60601-2-2; ANSI/AAMI/IEC 60601-2-2; CSA C22.2 NO. 60601-2-2 Medical electrical equipment - Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators IE
IEC 60601-2-2; EN 60601-2-2; DIN EN 60601-2-2; VDE 0750-2-2; IEC 60601-2-2 Edition 6.1 2023-02 CONSOLIDATED VERSION; IEC 60601-2-2 Edition 6.0 2017-03; ANSI AAMI IEC 60601-2-2:2017 Medical electrical equipment − Part 2-10: Parti
IEC 60601-2-2; IEC 60601-2-2 Edition 6.0 2017-03; IEC 60601-2-3; IEC 60601-2-4; IEC 60601-2-4 Edition 3.1 2018-02 Consolidated Version; IEC 60601-2-5; IEC 60601-2-5 Edition 3.0 2009-07 (The above standards exclude Clause 201.10.
IEC 60601-2-2:2017 (Section(s) 201.17/202) 1
IEC 60601-2-2 : 2018-12 Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hochfrequenz-Chirurgiegeräten (IEC 60601-2-2:2017); Deutsche Fassung EN IEC
IEC 60601-2-2 : 2018-12 ⊗ Medizinische elektrische Geräte - Teil 2-2: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Hochfrequenz-Chirurgiegeräten (IEC 60601-2-2:2017); Deutsche Fassung
IEC 60601-2-2:2017 6-389 IEC 60601-2-2 Edition 6.0 2017-03 6-389 IEC 60601-2-5 Edition 3.0 2009-07 12-205 IEC 60601-2-6 Edition 2.1 2016-04 6-423 IEC 60601-2-8 Edition 2.1 b:2015 12-301 IEC 60601-2-10 Edition 2.1 2016-04 17-16 IEC 60
IEC 60601-2-2; EN 60601-2-24; IEC 60601-2-24; EN 60601-2-47; EN 60669-2-1; IEC 60669-2-1; EN 60945; IEC 60945; EN 61000-6-1; IEC 61000-6-1; SANS 61000-6-1; EN 61000-6-2; IEC 61000-6-2; SANS 61000-6-2; EN 61000-6-3; IEC 61000-6-3; S
3 Exclusions Table Standard Clause Measurement/testing IEC 60601-1 9.5 Expelled parts Hazard 9.5.2 Cathode ray tubes. 9.7.5 Pressure vessels 11.2.2 ME Equipment and ME systems used in conjunction with. 11.4 ME Equipment and ME System
IEC 60601-2-2; EN IEC 60601-2-2; ANSI/AAMI/IEC 60601-2-2; CSA C22.2 NO. 60601-2-2 Medical electrical equipment – Part 2-18: Particular requirements for basic safety and essential performance of endoscopic equipment IEC 60601-2-18;
IEC 60601-2-2:2017 SIST EN 60601-2-2:2009 SIST EN 60601-2-2:2018 Medical electrical equipment - Part 2 -2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency
IEC 60601-2-2 Edition 6.0 2017-03 (excluding clauses listed in the “Exclusion” table above) 6-389 IEC 60601-2-18: Edition 3.0 2009-08 9-114 IEC 60601-2-22 Edition 4.0 2019-11 (excluding clauses listed in the “Exclusion” table above)
IEC 60601-2-2 : 2018-12 Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high-frequency surgical equipment (IEC 60601-2-2:2017); German version EN IEC 60601-2-2:2018 DIN
IEC 60601-2-2; Cardiac Defibrillators, Defibrillator-Monitors IEC 60601-2-4; Nerve and Muscle Stimulators IEC 60601-2-10; Hemodialysis Equipment IEC 60601-2-16; Endoscopic Equipment IEC 60601-2-18;
IEC 60601-2-2:2019/A1:2024, EN IEC 60601-2-2:2018+A1:2024, IEC 60601-2-2:2017/AMD1:2023 _ Par 04 - Prescrizioni generali/General requirements, Par 05 - Prescrizioni generali per le prove sugli apparecchi EM/General requirements for testin
IEC 60601-2-2 : 2017-03 Medical electrical equipmen t - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories IEC 60601-2-2 : 2009-02
IEC 60601-2-2 Edition 6.0 2017-03; ANSI/AAMI IEC 60601-2-2:2017 6-389 IEC 60601-2-20 Edition 3.0 2020-09 6-462 IEC 60601-2-22 Edition 4.0 2019-11; IEC 60601-2-22 Edition 3.1 2012-10 12-356 12-268 IEC 60601-2-25 Edition 2.0 2011-10;
IEC 60601-2-25 Edition 2.0, 2011-10 3-105 ANSI AAMI IEC 60601-2-25:2011/(R)2016 3-105 IEC 60601-2-27 Edition 3.0 2011-03 3-126 ANSI AAMI IEC 60601-2-27:2011(R)2016 3-126 IEC 60601-2-47 Edition 2.0 2012-02 3-155 ANSI AAMI IEC 60601-2-47