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ISO/IEC 17025 directory

IEC 60601-2-52 Accredited Testing Labs in Germany

9 laboratories in Germany are accredited by DAKKS under ISO/IEC 17025 to perform IEC 60601-2-52 testing. From the accredited scope text: “IEC 60601-2-52:2009 + Cor.:2010 + A1:2015); German version EN 60601-2-52:2010 + AC:2011 + A1:2015 DIN EN 60601-2-52 : 2010-12 ⊗ - Medical electrical equipment - Part 2-52: Particular requirements for” “IEC 60601-2-52 : 2009-12 Medical electrical equipme nt - Part 2-52: Particular requirements for basic safety and essential performance of medical beds + Amendment 1: 2015-03 IEC 60601-2-66 : 2015-06 ⊗” “IEC 60601-2-52:2009); Deutsche Fassung EN 60601-2-52:2010 VDE 0750-2-52:2010-12 DIN EN 60601-2-54 : 2020-03 Medizinische elektrische Geräte - Teil 2-54: Besondere Festlegungen für die Sicherheit und d”

Labs
9
Primary AB
DAKKS9 labs

Accredited Labs

UL International Germany

Neu-Isenburg, DE

Scope

Leistungsmerkmale von Geräten zur Stimulation von Nerven und Muskeln (IEC 60601-2-10:2012 + A1:2016); Deutsche Fassung EN 60601-2-10:2015 + A1:2016 DIN EN 60601-2-18 : 2016-10 Medizinische elektrisch e Geräte - Teil 2-18: Besondere Fes

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TÜV Technische Überwachung Hessen GmbH EMV-Labor

Kassel, DE

Scope

DIN EN 60601-2-47:2016-02 Medizinische elektrische Geräte - Teil 2-47: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von ambulanten elektrokardiographischen Systemen (IEC 60601-2-47:2012); De

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TÜV Rheinland Japan Ltd. Yokohama Laboratories Global Technology Assessment Center

Japan, DE

Scope

Department Standard / in house procedure / Version Title of standard or in house procedure (deviaBons /reducBons modificaBons of standard) LocaBon/ reducBons VDE 0750 -2-50: 2022 Product Safety IEC 60601 -2-52:2009 + A1:

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CSA Group Bayern

Plattling, DE

Scope

IEC 60601-2-52:2009); Deutsche Fassung EN 60601-2-52:2010 VDE 0750-2-52:2010-12 DIN EN 60601-2-54 : 2020-03 Medizinische elektrische Geräte - Teil 2-54: Besondere Festlegungen für die Sicherheit und die wesentlichen Leistungsmerkmale vo

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Entwicklungs- und Prüflabor Holztechnologie

Dresden, DE

Scope

DIN EN ISO 1923 1995-06 Cellular plastics and rubbers - Determination of linear dimensions DD DIN EN ISO 2439 2009-05 Flexible cellular polymeric materials - Determination of hardness (indentation technique) DD DIN

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TÜV SÜD Product Service

Frankfurt/Main, DE

Scope

Quellenverzeichnis Regelwerke/Prüfverfahren: DIN EN 1865-1 : 2015-08 Krankentransportmittel im K rankenkraftwagen - Teil 1: Allgemeine Krankentragesysteme und Krankentransportmittel; Deutsche Fassung EN 1865-1:2010+A1:2015 DIN EN ISO 10

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Eurofins Product Service

Reichenwalde, DE

Scope

IEC 60601-2-52 : 2009-12 Medical electrical equipme nt - Part 2-52: Particular requirements for basic safety and essential performance of medical beds + Amendment 1: 2015-03 IEC 60601-2-66 : 2015-06 ⊗ Medical electrical equipment - Part

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SLG Prüf- und Zertifizierungs

Hartmannsdorf, DE

Scope

IEC 60601-2-52:2009 + Cor.:2010 + A1:2015); German version EN 60601-2-52:2010 + AC:2011 + A1:2015 DIN EN 60601-2-52 : 2010-12 ⊗ - Medical electrical equipment - Part 2-52: Particular requirements for the basic safety and essential perfo

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TÜV Rheinland (Shanghai) Co.,

China, DE

Scope

IEC 60601-2-52:2009); German version EN 60601-2-52:2010 Medical Equipment # IEC 60601 -2-54:2022 Medical electrical equipment - Part 2 -54: Particular requirements for the basic safety and essential performance of X- ray equipment

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This page is a fixed slice of the register: every IEC 60601-2-52 scope we hold for Germany. Search narrows it further by city, accreditation body, or a term from the scope text itself.

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Top analytes for IEC 60601-2-52 in Germany

  • Hardness1
  • Radiation, Ionizing/Non-Ionizing1

About ISO/IEC 17025 in Germany

Deutsche Akkreditierungsstelle (DAKKS) is the primary accreditation body issuing ISO/IEC 17025 accreditation for testing laboratories in Germany.

ISO/IEC 17025 is the international standard for the competence of testing and calibration laboratories. Accreditation to this standard provides independent confirmation that a laboratory operates a quality management system and is technically competent to produce valid results within its declared scope.

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