IEC 62366-1 Accredited Testing Labs Worldwide
22 accredited laboratories in 8 countries hold IEC 62366-1 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation.
Available in 8 Countries
Top matrices for IEC 62366-1
Sample labs
IEC 62366-1; IEC 60601-1-8; IEC TR 62366-2; IEC 60601-1-11; IEC 60601-2-2; IEC 60601-2-10; IEC 60601-2-18; IEC 60601-2-22; IEC 60601-2-28 2; IEC 60601-2-36; IEC 60601-2-37; IEC 60601-2-43 2; IEC 60601-2-44 2; IEC 60601-2-45 2
IEC 62366-1; IEC 62366-1 Edition 1.1 2020-06 CONSOLIDATED VERSION; ANSI AAMI IEC 62366-1; ANSI AAMI IEC 62366-1:2015+AMD1:2020 (Consolidated Text); CSA IEC 62366-1; EN 62366-1 IEC 60601-1-3; IEC 60601-1-3:2008; IEC 60601-1-3 Editio
IEC 62366-1; IEC 80601-2-60 Edition 2.0 2019-06; AAMI/CSA 60601-1 ED 3.2; CAN/CSA-C22.2 No. 60601-1:14; JIS T 0601-1 OFF, Office (excluding Ionizing Measurement, Laser Testing) IEC 60950-1 ITAV, IT and AV equipment (excluding
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/AAMI/IEC 60601-1-8; CAN/CSA-C22.2 No. 60601-1-8; IEC 60601-1-11; EN 60601-1-11; ANSI/AAMI HA60601-1-11; CAN/CSA-C22.2 No. 60601-1-
Department Standard / in house procedure / Version Title of standard or in house procedure (deviaBons /reducBons modificaBons of standard) LocaBon/ reducBons Product Safety IEC 62262:2021 EN 62262/A1:2021 DIN EN 62262 :202
IEC 62366-1; CSA CEI/IEC 62304; CAN/CSA ISO 10079-1; CAN/CSA ISO 10079-2; CAN/CSA ISO 10079-3; CAN/CSA ISO 10079-4; CSA ISO 15197; GB/T 37704 Exclusions for IEC 60601-15, EN 60601-1, ANSI/AAMI ES 60601-15, CAN/CSA C22.2 No. 6060
IEC 62366-1; IEC 62304 (Ed. 1 + Am 1) Laboratory (excluding Vicat Softening and CRT/High Vacuum) IEC 61010-1, Ed. 2.0; EN 61010-1, Ed. 2.0; UL 61010-1, Ed. 2.0; CSA C22.2 No. 61010-1 Ed. 2.0; AS 61010-1 Ed. 2.0; ANSI/UL 61010-1
Test Technology: Test Method(s) 2,3,4: Part 4-2: Guidance and interpretation - Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems IEC TS 60601-4-2 Ophthalmic instruments — Fundam
IEC 62366-1; EN 62366-1; ANSI AAMI IEC 62366-1 1 When the date, edition, version, etc. is not identified in the scope of accreditation, laboratories may use the version that immediately precedes the current version for a period of o
IEC 62366-1; EN 62366- 1; CAN/CSA-IEC 62366-1; ANSI/AAMI/IEC 62366-1 Environmentally conscious design IEC 60601-1-9; EN 60601-1-9; CAN/CSA C22.2 No. 60601-1-9 Home healthcare environment IEC 60601-1-11; EN 60601-1-11; ANSI/AAM
IEC 62366-1:2007 + AMD1:2014) IEC 60601-1-6:2010 + AMD1:2013 + AMD2:2020 EN 60601-1-6:2010 +A1:2015 + A2:2021 (incl IEC 62366-1:2015 + AMD1:2020) F Alarm systems in medical Electrical safety IEC 60601-1-8:2006 + A1 F el
IEC 62366-1: 2015 + A1:2020) (incl EN 62366-1: 2015 +A1: 2020) Nerve and muscle stimulator EN60601-2-10:2015 G Exclusions: None Medical electrical equipment IEC 60601-1-11: 2015 C, G and medical electrical +A1;
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/AAMI/IEC 60601-1-8; CAN/CSA-C22.2 No. 60601-1-8; IEC 60601-1-11; EN 60601-1-11; ANSI/AAMI HA60601-1-11; CAN/CSA-C22.2 No. 6060
IEC 62366-1; EN 62366-1; CSA IEC 62366-1; ANSI/AAMI/IEC 62366-1 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance – Collateral standard: General requirements, tests and guidance
IEC 62366-1 Laboratory ANSI/UL 61010-1 3rd Ed, dated May 12, 2012, with revision through July 19, 2019; IEC 61010-1; EN 61010-1; IEC 61010-1 Edition 3.0 2010-06; IEC 61010-1 Edition 3.1 2017-01 (The above
IEC 62366-1; EN 62366-1; CSA IEC 62366-1; ANSI/AAMI/IEC 62366-1 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance – Collateral standard: General requirements, tests and guidance
IEC 62366-1:2015+A1:2020; EN 62366-1:2015+A1:2020; ANSI AAMI ES60601-1:2005/(R)2012 & A1:2012, C1:2009/(R)2012 & A2:2010/(R)2012 (Cons. Text) [Incl. AMD2:2021]; GB 9706.103-2020; IEC 60601-1-3:2008+A1:2013+A2:2021; EN 60601-1-3:2008+A
IEC 62366-1:2020 1.1 Edition; IEC 62304:2015 1.1 Edition; IEC 60601-1-12 Edition 1.1 2020-07 CONSOLIDATED VERSION; ANSI AAMI IEC 60601-1-12:2016 [Including AMD 1:2021]; CSA CAN/CSA-C22.2 No. 60601-1-12:15 + A1:21 Medical electrical eq
IEC 62366-1; IEC 62366-1:2015; ANSI/AAMI/IEC 62366-1; ANSI/AAMI/IEC 62366-1:2015; CAN/CSA-IEC 62366-1; CAN/CSA-IEC 62366-1:2015; EN 62366-1; EN 62366-1:2015; JIS T 62366-1; JIS T 62366-1:2019; Requirements/Guidelines fo
IEC 62366-1; ANSI/AAMI/IEC 62366-1
TUV Rheinland Italia S.r.l. Via Mattei 3 20005 Pogliano Milanese MI Allegato al certificato di accreditamento n. 00321 rev. 5 del 25/06/2025 UNI CEI EN ISO/IEC 17025:2018 Revisione: 72 Sede A Data: 29/09/2025 pag. 15 di 64 Emis
IEC 62366-1:15 (R2020) + A1:21; ISO 80601-2-12 First Edition 2011-04-15; EN ISO 80601-2-12 (2011); CAN/CSA-C22.2 No. 80601-2-12 (2012); IEC 80601-2-30 Edition 1.1 2013-07