IEC 60601-2-23 Accredited Testing Labs Worldwide
14 accredited laboratories in 4 countries hold IEC 60601-2-23 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle.
Available in 4 Countries
Sample labs
IEC 60601-2-23 : 2011-02 Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment IEC 60601-2-26 : 2012-05⊗ Medical electrica
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 60601-2-23:2011-02 Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment IEC 60601-2-23:1999-12⊗ - Medical electrical
IEC 60601-2-23 (Excluding Cl 201.17, 202); IEC 60601-2-24 (Excluding Cl 201.11.6.3, 201.11.6.5, 201.17, 202); IEC 60601-2-25 (Excluding Cl 201.17, 202); IEC 60601-2-26 (Excluding Cl 201.17, 202); IEC 60601-2-27 (Excluding Cl 201.17,
This document is a translation. The definitive version is the original German annex to the accreditation certificate. DIN EN 60601-2-23 : 2016-08 Medizinische elektrische Geräte – Teil 2 -23: Besondere Festlegungen für die Sicherheit
IEC 60601-2-23 Edition 3.0 2011-02; IEC 60601-2-25 Edition 2.0 2011-10; ANSI AAMI IEC 60601-2-25:2011/(R)2016; IEC 60601-2-27 Edition 3.0 2011-03; ANSI AAMI IEC 60601-2-27:2011(R)2016; IEC 60601-2-28 Edition 3.0 2017-06; IEC 80601-2-3
IEC 60601-2-23:2011); Deutsche Fassung EN 60601-2-23:2015 VDE 0750-2-23 : 2016-08 DIN EN 60601-2-23 : 2000-11 ⊗ - Medizinische elektrische Geräte - Teil 2-23: Besondere Festlegungen für die Sicherheit einschließlich wesentlicher Leist
IEC 60601-2-23 Edition 3.0 2011-02 1-87 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 60601-2-28 Edition 3.0
IEC 60601-2-23 Edition 3.0 2011-02 (clause 202 only) 1-87 IEC 60601-2-25 Edition 2.0 2011-10 (clause 202 only) 3-105 IEC 60601-2-27 Edition 3.0 2011-03 (clause 202 only) 3-126 IEC 60601-2-31 Edition 2.1 2011-09 (clause 202 only) 3-102 I
IEC 60601-2-23:2011);
IEC 60601-2-23 Edition 3.0 2011-02 (Section(s) 201.17/202) 1; IEC 60601-2-25 Edition 2.0 2011-10 1; ANSI AAMI IEC 60601-2-25:2011/(R)2016 1; ANSI AAMI IEC 60601-2-25 Edition 2.0 2011-10 (Section(s) 201.17/202); ANSI AAMI IEC 60601-2-2
IEC 60601-2-23 : 2011-02 IEC 60601-2-24 : 2012-10 IEC 60601-2-25 : 2011-10 IEC 60601-2-26 : 2012-050 IEC 60601-2-31 : 2020 IEC 60601-2-33 : 2010-03 K DAkkS Deutsche Akkreditierungsstelle Medical electrical equipment - Part 2-19: Particular
IEC 60601-2-23 (Transcutaneous Partial Pressure Monitoring Equipment); EN/IEC 60601-2-24 (Infusion Pumps and Controllers); EN/IEC 60601-2-25 (Electrocardiographs); EN/IEC 60601-2-26 (Electroencephalographs); EN/IEC 60601-2-27 (Electroc
IEC 60601-2-23 Edition 3.0 2011-02 1-87 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