IEC 80601 Accredited Testing Labs Worldwide
IEC 80601, all parts. Each lab card shows which parts it holds.
- IEC 80601-2-3Part 2-31 lab →
- IEC 80601-2-12Part 2-121 lab →
- IEC 80601-2-26Part 2-2625 labs →
- IEC 80601-2-30Part 2-3043 labs →
- IEC 80601-2-35Part 2-3512 labs →
- IEC 80601-2-49Part 2-4932 labs →
- IEC 80601-2-55Part 2-552 labs →
- IEC 80601-2-58Part 2-5814 labs →
- IEC 80601-2-59Part 2-599 labs →
- IEC 80601-2-60Part 2-6038 labs →
- IEC 80601-2-61Part 2-614 labs →
- IEC 80601-2-69Part 2-692 labs →
Show all 15 parts
- IEC 80601-2-71Part 2-711 lab →
- IEC 80601-2-77Part 2-7719 labs →
- IEC 80601-2-78Part 2-7810 labs →
68 accredited laboratories in 13 countries hold IEC 80601 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle. In the register, IEC 80601 scope entries most often cover Blutdruck, Body Temperature, Lithium-Ion in Medical equipment, electrical safety and EMC, Glass.
Available in 13 Countries
Top matrices for IEC 80601
Top analytes for IEC 80601
- Blutdruck (1)
- Body Temperature (1)
- Lithium-Ion (1)
Sample labs
(A2LA Certificate No. 0751.05) Revised 03/02/2026 Page 3 of 10 Test Technology: Test Method(s) 1, 2: EMC Medical (continued) IEC/EN 60601-2-25 (cl. 202 only); IEC/EN 60601-2-27 (cl. 202 only); IEC/EN 60601-2-31 (cl. 202 only); IEC/EN
IEC 80601-2-71:2018-12 Medical electrical eq uipment - Part 2-71: Particular requirements for the basic safety and essential performance of functional oximetry devices (IEC 80601-2-71:2015); German version EN IEC 80601-2-71:2018 VDE 075
IEC 80601-2-30 : 2020-03 Medizinische elekt rische Geräte –Teil 2-30: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von automatisierten nicht-invasiven Blutdruckmessgeräten (IEC 80601-2-30:2
IEC 80601 -2-30:2009 +AMD1:2013 SIST EN 80601-2-30:2010+ +AMD1:2015 IEC 80601-2-30:2018 SIST EN 80601-2-30:2019 Medical electrical equipment - Part 2 -30: Particular requirements for basic safety and essential performance of automa
IEC 80601-2-77 Edition 1.0 2019-07 6-438 3 This laboratory is only accredited for testing ac tivities outlined within the test methods listed above. Reference to any other activity with in these standards, such as risk management or ri
IEC 80601-2-77 Edition 1.0 2019-07 6-438 ISO 80601-2-79 First Edition 2018-07 1-143 IEC TR 60601-4-2 Edition 1.0 2016-05 19-19 IEC TS 60601-4-2 Edition 1.0 2024-03 19-50 1These methods have been assessed by A2LA according to A2LA’s F
IEC 80601-2-49:2018 Ed.1.0 (Only Section 202.8.102); AIM Standard 7351731 Rev. 3.00 2021-06-04 (Only Annex A, B, C and D devices only) EMC – Commercial Unintentional Radiated & Conducted Emissions CISPR 11:2015 +A1:2016 & A2:2019;
IEC 80601-2-12:2011 + Cor. :2011); German version EN ISO 80601-2-12:2011 + AC:2011 ⊗ DIN EN IEC 80601-2-26 : 2022-04 Medical electrical equipment - Part 2-26: Particular requirements for the basic safety and essential performance of el
IEC 80601-2-49:2018; EN IEC 60601-2-49:2019; Safety of Medical Beds IEC 60601-2-52:2009 + A1:20151; EN 60601-2-52:2010 + A1:2015; Respiratory Gas Monitors ISO 80601-2-55:20181; EN ISO 80601-2-55:2018; Clinical Thermometers for Body Tem
IEC 80601-2-60:2020, IEC 80601-2-60:2019 _ Par 04 - Prescrizioni generali/General requirements, Par 05 - Prescrizioni generali per le prove sugli apparecchi EM/General requirements for testing ME Equipment, Par 06 - Classificazione degli
IEC 80601 -2-30:2018 Medical electrical equipment - Part 2 -30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers Medical Equipment EN IEC 80601 -2-30:2019
IEC 80601-2-26 Medical electrical equipment - 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 Medical electrical
IEC 80601-2-26:2022-04 Medizinische elektris che Geräte - Teil 2-26: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Elektroenzephalographen (IEC 80601-2- 26:2019); Deutsche Fassung EN IEC 8
IEC 80601-2-30:2009 EN 80601-2-30:2010 IP, S Medical electrical equipment Heating devices using blankets, pads and mattresses and intended for heating in medical use. Electrical safety IEC 80601-2-35:2009+A1:2016 EN 80601
IEC 80601-2-30 Edition 2.0 2018-03; ANSI/AAMI IEC 80601-2-30:2018 3-123 IEC 60601-2-35 Edition 2.0 2020-09 6-483 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 2017-1
IEC 80601-2-30:2009 (Excluding Sections 201.106, 202.6.2.102); IEC 80601-2-30:2009 + A1:2013 (Excluding Sections 201.106, 202.6.2.102); IEC 80601-2-30:2018 (Excluding Sections 201.106, 202.6.2.102); CAN/CSA-C22.2 No. 80601-2-30:19 (Ex
IEC 80601-2-30 Edition 1.1 2013-07 3-123 ANSI AAMI IEC 80601-2-30:2018 3-123 IEC 60601-2-34 Edition 3.0 2011-05 3-115 ANSI AAMI ES60601-1:2005/(R)2012 & A1:2012, C1:2009/(R)2012 & A2:2010/(R)2012 (Cons. Text) [Incl. AMD2:2021 19-46 IE
IEC 80601-2-30, Clause 202 of EN IEC 80601-2-30, Clause 202 of IEC 60601-2-37, Clause 202 of EN 60601-2-37, Clause 202 of IEC 80601-2-49, Clause 202 of EN IEC 80601-2-49, Clause 202 of ISO 80601-2-55, Clause 202 of EN ISO 80601
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