IEC 60601-1 Accredited Testing Labs Worldwide
84 accredited laboratories in 14 countries hold IEC 60601-1 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle, United Kingdom Accreditation Service. In the register, IEC 60601-1 scope entries most often cover Audible Acoustic Emissions, Combustible Gasses, Rf Exposure in Medical equipment, electrical safety and EMC, Water, Electronic.
Available in 14 Countries
Top matrices for IEC 60601-1
Top analytes for IEC 60601-1
- Audible Acoustic Emissions (1)
- Combustible Gasses (1)
- Rf Exposure (1)
- Temperature (1)
Sample labs
IEC 60601-1, ANSI AAMI ES60601-1 also apply to other collaterals and particulars in the 60601/80601 family of standards except where otherwise stated. Exclusions Table Standard Clause/Description IEC 60601-1 EN 60601-1 ANSI/AAMI ES6
IEC 60601-1 Audio/Video, Information and Communication Technology Equipment IEC 62368-1; EN 62368-1; EN IEC 62368-1; BS EN 62368-1; BS EN IEC 62368-1; J 62368-1; AS/NZS 62368-1; UL 62368-1; CAN/CSA-C22.2 No.62368-1; CNS 15598-1;
IEC 60601-1 (2005) + A1 (2012)+ A2 (2020); ANSI/AAMI ES60601-1:2005/ A2:2021; IEC 60601-1:2005/A2:2020; IEC 60601-1-2, Ed. 4.0 (2014) + A1 (2020); ANSI/AAMI/IEC 60601-1-2:2014/ A1:2021; BS EN 60601-1-2:2015+A1:2021; IEC 60601-1-2, Ed.
IEC 60601-1:2005 + Cor1:2006 + Cor2:2007 + A1:2012 + A1:2012/Cor1:2014 + A2:2020); Deutsche Fassung EN 60601-1:2006 + Cor.:2010 + A1:2013 + AC:2014 + A1:2013/AC:2014 + A12:2014 + A2:2021 DIN EN 60601-1 : 2013-12 - Medizinische elektrisc
IEC 60601-1; IEC 60601-1:1988; IEC 60601-1:1988/AMD1:1991; IEC 60601-1:1988/AMD2:1995; IEC 60601-1-1:2000; IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION; ANSI AAMI ES60601-1; ANSI AAMI ES60601-1:2005/(R)2012 & A1:2012, C1:200
IEC 60601-1; IEC 60601-1-1; IEC 60601-1-11; IEC 60601-1-12; IEC 60601-1-3; IEC 60601-1-4; IEC 60601-1-8; IEC 60601-2-10; IEC 60601-2-18; IEC 60601-2-2; IEC 60601-2-23; IEC 60601-2-25; IEC 60601-2-26; IEC 60601-2-27; IEC 60601-
IEC 60601-1; IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION; IEC 60601-1-1; IEC 60601-1-3; IEC 60601-1-3 Edition 2.2 2021-01 CONSOLIDATED VERSION; IEC 60601-1-4; IEC 60601-1-6; IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED
IEC 60601-1; EN 60601-1; ANSI/AAMI ES60601-1; CAN/CSA-C22.2 No. 60601-1; IEC 60601-1-6; EN 60601-1-6; CAN/CSA-C22.2 No. 60601-1-6; IEC 62366-1; EN 62366-1; CAN/CSA-IEC 62366-1; ANSI/AAMI/IEC 62366-1; IEC 60601-1-8; EN 60601-1-8; ANSI
IEC 60601-1:2005/AMD2:2020 (Active) Excluded: cl. 8.8.4.2 Oxygen Aging for Rubber Insulation Parts cl. 9.5.2 Cathode Ray Tubes cl. 10.1.1 X-radiation cl. 11.2.2 Oxygen enriched atmospheres cl. 11.3 Constructional requirements for
IEC 60601-1; EN 60601-1; CAN/CSA-C22.2 No. 60601-1; IEC 60601-1:2005 + A1 (2012); IEC 60601-1:2005+AMD1:2012+AMD2:2020; ANSI/AAMI ES60601-1; ANSI/AAMI ES60601-1:2005/A2:2021; ANSI/AAMI ES60601-1:2005/(R)2012 & A1:2012, C1:2009/(R)201
IEC 60601-1:2005 + Cor. :2006 + Cor. :2007 + A1:2012); Deutsche Fassung EN 60601- 1:2006 + Cor. :2010 + A1:2013 DIN EN 60601-1 : 2007-070 - Medizinische elektrische Geräte - Teil 1: Allgemeine Festlegungen für die Sicherheit einschließlich
IEC 60601-1-3:2008/ A2:2021 EN 60601-1-3:2008 + A1:2013 EN 60601-1- 3:2008/A2:2021 DIN EN 60601-1-3:2014- 06 VDE 0750-1-3:2014-6 Medical electrical equipment - Part 1-3: General requirements for basic safety and essenDal performanc
IEC 60601-15, EN 60601-1, ANSI/AAMI ES 60601-15, CAN/CSA C22.2 No. 60601-1 Cl. 8.8.4.2 Rubber ageing test Cl. 9.5.2 Cathode ray tubes Cl. 11.7 Biocompatibility
IEC 60601-1:2005 + Cor. :2006 + Cor. :2007 + A1:2012); Deutsche Fassung EN 60601 -1:2006 + Cor. :2010 + A1:2013 VDE 0750-1:2013-12 DIN EN 60601-1-2 : 2022-01 Medizinische elektrische Geräte - Teil 1 -2: Allgemeine Festlegungen für die
IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION; IEC 60601-1-2 Edition 4.1 2020-09 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-2:2014 [Including AMD 1:2021]; IEC 60601-1-3 Edition 2.2 2021-01 CONSOLIDATED VERSION; IEC 60601-1-6 Edi
IEC 60601-1:2005 + Cor1:2006 + Cor2:2007 + A1:2012 + A1:2012/Cor1:2014 + A2:2020); Deutsche Fassung EN 60601-1:2006 + Cor.:2010 + A1:2013 + AC:2014 + A1:2013/AC:2014 + A12:2014 + A2:2021
IEC 60601-1 : 2005-12 Medical electrical equipment – Part 1: General requirements for basic safety and essential performance + Corrigendum 1: 2006-12 + Corrigendum 2: 2007-12 + Amendment 1: 2012-07 + Amendment 2: 2020-08 IEC 60601-2-1
IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION (excluding Cl. 9.5.2 Cathode ray tube test; Cl. 10.4 LED test per IEC 62471 Cl.11.4, flammable anesthetic mixtures test; Cl. 15.4.3.4 Lithium battery test per IEC 62133-2 or IEC 60086-4
IEC 60601-1:2005 + Cor1:2006 + Cor2:2007 + A1:2012 + A1:2012/Cor1:2014 + A2:2020); Deutsche Fassung EN 60601- 1:2006 + Cor.:2010 + A1:2013 + AC:2014 + A1:2013/AC:2014 + A12:2014 + A2:2021 VDE 0750-1:2022-11 DIN EN 60601-1 : 2013-12 ⊗ -
IEC 60601-1; EN 60601-1; BS EN 60601-1; UL60601-1; AS/NZS IEC 60601.1
IEC 60601-1:1988/AMD2:1995; IEC 60601-1:2005+A1:2012; IEC 60601-1:2005+A1:2012+A2:2020; ES60601-1:2005/(R)2012 and A1:2012 C1:2009/(R)2012 and A2:2010/(R)2012 (Consolidated Text); IEC 60601-1-4:1996/AMD1:1999; IEC 60601-1-6:2010+A1
21.102 Abrasion test for current-carrying hose 21.103 Flexing test for current-carrying hose 21.104 Torsion test for current-carrying hose IEC/EN 60335-2-59 32 UV radiation IEC/EN 60335-2-65 32.101 Ozone concentration 32.102 UV radi
IEC 60601-1; GB 9706.1:2020; GB 9706.1-2007; GB 9706.15-2008; UL/CSA/IEC/EN 60601-1 (inclusive of all collateral standards); UL/CSA IEC/EN 60601-2 (All Inclusive); IEC/ISO 80601-2 CSA 80601-2 (All Inclusive); IEC/EN 60601-1-4; IEC
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 4-262 ISO 80601-2-56 Second Edition 2017-03 6-421 ISO 80601-2-61 Second Edition 2017-12 (Corrected Ve
IEC 60601-1:2005 + Cor1:2006 + Cor2:2007 + A1:2012 + A1:2012/Cor1:2014 + A2:2020); Deutsche Fassung EN 60601-1:2006 + Cor.:2010 + A1:2013 + AC:2014 + A1:2013/AC:2014 + A12:2014 + A2:2021 DIN EN 60601-1 : 2013-12 ⊗ - Medizinische elektr
IEC 60601-1; EN 60601-1; BS EN 60601-1; ANSI/AAMI ES60601-1; CAN/CSA-C22.2 NO. 60601-1; AS/NZS IEC 60601.1; JIS T 0601-1 Usability IEC 60601-1-6; EN 60601-1-6; BS EN 60601-1-6; CAN/CSA-C22.2 No 60601-1-6; AS IEC 60601.1.6; JIS
T298/M23/2025 Liite 1 / Appendix 1 Sivu / Page 21(23) Vaatimus/Requirement SFS-EN ISO/IEC 17025:2017 17.12.2025 Päätöksen päiväys / Date of decision 22.07.2028 Päätöksen viimeinen voimassaolopäivä / Date of expiry www.finas.fi Voimas
IEC 60601-1: 2005-12 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance + Corrigendum 1 : 2006-12 + Corrigendum 2 : 2007-12 + Amendment 1 : 2012-07 + Amendment 2 : 2020-08 IEC 60601
IEC 60601-1; EN 60601-1; BS EN 60601-1; AS/NZS60601.1; AS/AAMI ES60601-1; CAN/CSA-C22.2 No. 60601-1:14; IEC 60601-1-6; EN 60601-1-6; EXCLUDED MEASUREMENTS: - Not accredited for RISK ASSESSMENT 3 - Defibrillation protection - Pres
IEC 60601-1; EN 60601-1; ANSI/AAMI ES60601-1; CAN/CSA-C22.2 NO. 60601-1 Medical Electrical Equipment - Part 1-6: General Requirements for Basic Safety and Essential Performance - Collateral Standard: Usability IEC 60601-1-6; EN 60
IEC 60601-1; EN 60601-1 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance ANSI /AAMI ES60601-1 Medical electrical equipment - Part 1: General requirements for basic safety and e
IEC 60601-1; EN 60601-1; ANSI/AAMI ES60601-1; CAN/CSA-C22.2 No. 60601-1; JIS T 0601-1; AS/NZS 3200.1.0 (including on-site test) Radiation protection in diagnostic X-ray equipment IEC 60601-1-3; EN 60601-1-3; CAN/CSA C22.2 No. 6060
IEC 60601-1 : 1988 +A1 : 1991 +A2 : 1995); Deutsche Fassung EN 60601-1 : 1990 + A1 : 1993 + A2 : 1995 VDE 0750-1:1996-03 DIN EN 60601-1-1 : 2002-08⊗ Medizinische elektrische Geräte - Teil 1-1: Allgemeine Festlegungen für die Sicherheit
Test Technology: Test Method(s) 1, 2: Intentional Radiators (Using ANSI C63.4:2014, ANSI C63.26:2015; ANSI C63.27, and ANSI C63.10:2013 up to 40 GHz; excluding HAC and SAR unless otherwise noted) (cont.) KS X 3124; KS X 3137;
IEC 60601-1 : 2005-12 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance + Corrigendum 1 : 2006-12 + Corrigendum 2 : 2007-12 + Amendment 1 : 2012-07 + Amendment 2 : 2020-08 IEC 60601
IEC 60601-1 :2005+AMD2 :2020 EN 60601-1:2006+A12:2014 (Withdrawn) IEC 60601-1:1988 Amd A1 and A2 (Withdrawn) UL 60601-1:2003 (Withdrawn) All excluding IEC 60601-1-4 referred to in Sub-clause 52.1, also Section 6 (Clause 37 to 41) an
IEC 60601-1:2005 +A1:2012 IEC 60601-1:2005 +A1:2012 + AMD2:2020 Equipment, except those Excluding: 8.8.4.2 (environmental stress) 8.11.1e (supply mains switch) 9.6.2.1 (noise measurement) 9.6.3 (hand transmitted v
IEC 60601-1:2005 + Cor1:2006 + Cor2:2007 + A1:2012 + A1:2012/Cor1:2014 + A2:2020); Deutsche Fassung EN 60601-1:2006 + Cor.:2010 + A1:2013 + AC:2014 + A1:2013/AC:2014 + A12:2014 + A2:2021 VDE 0750-1: 2022-11 DIN EN 60601 -1: 2013 -12 ⊗
IEC 60601-1:2005+A1:2012, A2:2020 Excluding: cl. 8.5.5 Defibrillation proof applied parts cl. 8.8.4.2 Ageing of Rubber cl. 8.9.1.7 Material group classification testing cl. 8.9.3.4 Thermal cycling of potted or cemented parts 9.4
IEC 60601-1: 2005 + A1: 2012 +A2: 2020 Excluding: 8.5.5.1: Defibrillation protection Medical Electrical Equipment 8.5.5.2: Energy reduction test 8.8.3: Electric strength test above 10kV r.m.s, 5kV d.c 8.8.4.2: R
IEC 60601-1; EN IEC 60601-1; UL 60601-1
IEC 60601-1:2005 + Cor1:2006 + Cor2:2007 + A1:2012 + A1:2012/Cor1:2014 + A2:2020); Deutsche Fassung EN 60601-1:2006 + Cor.:2010 + A1:2013 + AC:2014 + A1:2013/AC:2014 + A12:2014 + A2:2021 VDE 0750-1:2022-11 DIN EN 60601-1 : 2013-12 ⊗
IEC 60601-1; EN 60601-1; ANSI/AAMI ES60601-1; CAN/CSA-C22.2 No. 60601-1; IEC 60601-1-6; EN 60601-1-6; CAN/CSA-C22.2 No. 60601-1-6; IEC 62366; EN 62366; ANSI/AAMI/IEC 62366; CAN/CSA-IEC 62366; IEC 62366-1; EN 62366-1; CAN/CSA-
Przedmiot badań/wyrób Rodzaj działalności/badane cechy/metoda Dokumenty odniesienia Urządzenia techniki fonicznej/wizyjnej, informatycznej i telekomunikacyjnej Badanie narażenia na światło łuku ksenonowego PN-EN IEC 62368-1:2020-11
IEC 60601-1, EN 60601-1; ANSI/AAMI ES60601-1; CAN/CSA-C22.2 No. 60601-1 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance – Collateral standard: Radiation protection in diagnosti
IEC 60601-1; ANSI/AAMI ES60601-1:2005/A2:2021 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements BS EN 61010-1; IEC 61010-1 Medical electrical equipment - Part
IEC 60601-11, Sect. 10.1 3.a, b, d; ST/SG/AC.10/11, Sect. UN 38.3 T4 Packaged Drop Test/ Unpackaged Drop Test Requirements of Standard Telcordia GR-63-CORE; GR-487-CORE; GR-950-CORE; GR-3108-CORE; ETSI EN 300 019; MIL-PRF 288
IEC 60601-1, EN 60601-1 IEC 60601-1-1, EN 60601-1-1 IEC 60601-1-3, EN 60601-1-3 IEC 60601-1-4, EN 60601-1-4 IEC 60601-1-6, EN 60601-1-6 IEC 60601-1-8, EN 60601-1-8 IEC 60601-1-9, EN 60601-1-9 IEC 60601-1-10, EN 60601-1-10 IEC 60601-
IEC 60601-1; EN 60601-1; DIN EN 60601-1; VDE 0750-1-1; ANSI AAMI ES60601-1:2005/(R)2012 and A1:2012, C1:2009/(R)2012 and A2:2010/(R)2012 (Consolidated Text); ANSI AAMI ES 60601-1:2005/(R)2012 & A1:2012 C1:2009/(R)2012 &
IEC 60601-1; EN 60601-1; IEC 60601-1 Edition 3.2 2020-08 Consolidated Version (The above standards exclude 60601-1: Clause 9.5.2 Cathode Ray Tubes, Clause 11.4 MEE and MES intended for use with flammable anaesthetics, Cla
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