IEC 60601-1 Accredited Testing Labs Worldwide

IEC 60601-1:2005+IEC 60601- 1:2005/AMD1:2012+IEC 60601- 1:2005/AMD2:2020 EN 60601-1:2006+EN 60601- 1:2006/corrigendum Mar.2010+EN 60601-1:2006/A1:2013+EN 60601- 1:2006/A12:2014+EN 60601- 1:2006/A2:2021 PN-EN 60601-1-11:2015- 09+A1:2021

IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION 19-49 IEC TR 60601-4-2 Edition 1.0 2016-05 19-19 IEC TS 60601-4-2 Edition 1.0 2024-03 19-50 IEC 60601-1-2 Edition 4.1 2020-09 CONSOLIDATED VERSION 19-36 ANSI AAMI IEC 60601-1-2:2014 [

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 elekt

IEC 60601-1 Drop IEC 60601-1 Impact IEC 60601-1 Temperature Altitude2 Up to 100,000 Feet (-72 to 150) °C MIL-STD-202 E, F, G, (Method 105); MIL-STD-810 Base, A, B, C, D, E, F, G, H, (Method 500); RTCA/DO-160 B, C, D, E, F, G, (Sec

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 Systems intended for use with flammable anaesthetics 11.6.5 I

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: Usability IEC 60601-1-6;EN 60601-1

IEC 60601-1; EN 60601-1 Power Transformers, Power Supplies, Reactors and Similar Products IEC 61558-1; IEC 61558-2-5; IEC 61558-2-6; IEC 61558-2-9; IEC 61558-2-15; IEC 61558-2-16; EN 61558-1; EN 61558-2-5; EN 61558-2-6; EN 61558-2-

IEC 60601-1:2005 + A2:2020 Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment Safety tests IEC/EN 60601-1-11: 2015 Medical electrical equipment Saf

IEC 60601-1:2005 + Cor. :2006 + Cor. :2007 + A1:2012); German version EN 60601-1:2006 + Cor. :2010 + A1:2013 DIN EN 60601-1:2007-07 ⊗ - Medical electrical equipment – Part 1: General requirements for basic safety and essential performa

IEC 60601-1) Vedere elenco dei dettagli delle prove flessibili/See list of flexible scope details _ Apparecchiature per radiocomunicazione/Radiocommunications Apparatus Denominazione della prova / Campi di prova Metodo di prova Tecnic

IEC 60601-1:2005+A1:2012(E) Clause 9.6.2.1. (The property determined from measurement is the average sound pressure level in a single position) Safety Tests Portable medical electrical equipment Hand-transmitted vi

IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION 19-49 IEC 60601-1-6 Edition 3.2 2020-07 CONSOLIDATED VERSION 5-132 IEC 60601-2-2 Edition 6.0 2017-03 (excluding clauses listed in the “Exclusion” table above) 6-389 IEC 60601-2-18:

IEC 60601-1; EN 60601-1; BS EN 60601-1; AS/NZS IEC 60601.1; GB 9706.1 I NFORMATION TECHNOLOGY Test Technology: Test Method(s)1,2: Cybersecurity Common security requirements for radio equipment - Part 1: Internet connected radio equ

Przedmiot badań/wyrób Rodzaj działalności/badane cechy/metoda Dokumenty odniesienia Medyczne urządzenia elektryczne Szczeliny w ochronie przed  zagrożeniami mechanicznymi Zakres: (0,1 - 1000) mm Metoda: pomiar wielkości liniowych PN

IEC 60601-1 Exclusions: 8.8.4.2 (environmental stress) 8.11.1e (supply mains switch) 9.6.3 (hand transmitted vibration) 10.1 (x-rays) 10.4 (laser and LED emissions) 10.5 (Other visible electromagnetic radiation) 10.6 (Infra-red

IEC 60601-1:2005 + Cor1:2006 + Cor2:2007 + A1:2012 + A1:2012/Cor1:2014 + A2:2020); German version EN 60601-1:2006 + Cor.:2010 + A1:2013 + AC:2014 + A1:2013/AC:2014 + A12:2014 + A2:2021 DIN EN 60601-1 : 2013-12 ⊗ - Medical electrical equ

IEC 60601-1, Edition 3.2 Series Test Technology: Test Method(s) 2, 3, 4: National / Regional Variation(s) 2, 3, 4: Medical Electrical Equipment– Part 1: General Requirements for Basic Safety and Essential performance (excludin

Nemko S.p.A. a socio unico Via del Carroccio, 4 20853 Biassono MB Allegato al certificato di accreditamento n. 00036 rev. 4 del 23/01/2025 UNI CEI EN ISO/IEC 17025:2018 Revisione: 35 Sede A Data: 15/10/2025 pag. 9 di 40 EN IEC

IEC 60601-1 Edition 3.2 2020-08 Clauses 4-9, 11- 16; ANSI AAMI ES60601-1:2005/(R)2012 and A1:2012, C1:2009/(R)2012 and A2:2010/(R)2012 3 Medical Electrical Equipment- Part 2-5: Particular Requirements for the Basic Safety and Essent

IEC 60601-1 (2012); UL 60601-1 (2006); EN 60601-1 (2006+A1:2013); IES 60601-2-22 (2007+A1:2012); EN 60601-2-22 (2013); IEC 60601-1-9 (2007) IEC 60601-1-12 (2014); IEC 60601-2-37 (2015); IEC TR 60601-4-2 (2016); CAN/CSA C22.2 No. 60601-1

Department Standard / in house procedure / Version Title of standard or in-house procedure (deviations / modifications of standard) Test area / reductions Medical Equipment IEC 60601 -1:2005 +A1:2012 +A2:2020 Medi

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

White Lab S.r.l. - Test'ing Via del Consorzio, 41 60015 Falconara Marittima AN Allegato al certificato di accreditamento n. 01044 rev. 7 del 21/05/2025 UNI CEI EN ISO/IEC 17025:2018 Revisione: 25 Sede A Data: 21/05/2025 pag. 5 d

IEC 60601-1; ANSI/AAMI ES60601-1 Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment IEC 60601-1-3 Medi

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 +AMD1:2012+AMD2:2020 Excluding: Clause 11.7 Biocompatibility Clause 8.8.42 Ageing of Rubber Annex’s G2, to G6 BS EN 60601-1:1990, Amds 1 to 3 IEC 60601-1:1988, Amds 1 and 2 Excluding: Anaesthetic Proof equipment

IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION; ANSI/AAMI ES60601-1:2005/(R)2012 & A1:2012, C1:2009/(R)2012 & A2:2010/(R)2012 (Cons. Text) [Incl. AMD2:2021] 19-49 19-46 IEC 60601-1-10 Edition 1.2 2020-07 CONSOLIDATED VERSION 19-3

IEC 60601-1:2005 + A1:2012 + A2:2020 (Excluding Sections 8.8.4.2 (rubber aging), 8.9.1.7, 9.5.2, 9.6.3, 10.1, 10.3, 11.2.2, 11.2.3, 11.4, 11.6.7, 11.7, 15.4.2 f, 15.4.3.4, 17, Annexes G and L); ANSI/AAMI ES60601-1:2005/(R)2012 & A1:201

Edition 19, 28/01/2026 50dB - 130dB radiation) 12.3 (UV radiation) 12.5.2 (ultrasonic pressure) 12.6 (laser sources) A,V,Hz,m,

IEC 60601-1:2005 + A1:2012 + A2:2020; EN 60601-1:2006 + A11:2011 + A1:2013 + A12:2014; CAN/CSA-C22.2 No. 60601-1-08; ANSI/AAMI ES60601 + A1:2005; JIS T 0601-1:2012 + A1:2014; JIS T 0601-1:2017 (Excluding cl.10.1) Safety Requirements f

IEC 60601-1, 1-6, 1-8, 1-11, 2-1, 2-5, 2-10, 2-22, 2-24, 2-25, 2-26, 2-27, 2-38, 2-40, 2-47 AP v. Batteries (BATT) IRN 507 EN-IEC 60086-4 AP

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. 10 di 64 Appa

IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION 19-49 ANSI/AAMI HA60601-1-11:2015 19-16 IEC 60601-1-11 Edition 2.1 2020-07 CONSOLIDATED VERSION 19-38 IEC 60601-1-2 Edition 4.1 2020-09 CONSOLIDATED VERSION 19-36 ANSI AAMI IEC 60601

IEC 60601-1; EN 60601-1; BS EN 60601-1; ANSI/AAMI ES60601-1; CSA C22.2 No. 60601-1