EN 60601-2-37:2001

Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment

Establishes particular requirements for the safety of ultrasonic diagnostic equipment and those aspects thereof which are directly related to safety. Does not cover ultrasonic therapeutic equipment; however, equipment used for the imaging of body structures by ultrasound in conjunction with therapeutic modalities is covered.

Medizinische elektrische Geräte - Teil 2-37: Besondere Festlegungen für die Sicherheit von Ultraschall-Geräten für die medizinische Diagnose und Überwachung

Appareils électromédicaux - Partie 2-37: Règles particulières de sécurité pour les appareils de diagnostic et de surveillance médicaux à ultrasons

Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment (IEC 60601-2-37:2001)

General Information

• Status: Withdrawn
• Publication Date: 16-Oct-2001
• Withdrawal Date: 30-Sep-2004
• ICS: 11.040.55 - Diagnostic equipment
• ICS: 17.140.50 - Electroacoustics
• Technical Committee: CLC/TC 62 - Electrical equipment in medical practice
• Drafting Committee: IEC/SC 62B - IEC_SC_62B
• Parallel Committee: IEC/SC 62B - IEC_SC_62B
• Current Stage: 9960 - Withdrawal effective - Withdrawal
• Start Date: 01-Oct-2010
• Completion Date: 01-Oct-2010
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Mandate: M/023 - Standardization mandate to CEN/CENELEC concerning the development of European standards relating to medical devices
• Mandate: M/432 - Standardisation Mandate addressed to CEN and CENELEC within the framework of Directive 2007/47/EC amending Directive 90/385/EEC and Directive 93/42/EEC relating to Medical Devices
• Ref Project: SIST EN 60601-2-37:2002 - Medical electrical equipment -- Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment

Relations

• Replaced By: EN 60601-2-37:2008 - Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment
• Effective Date: 28-Jan-2023
• Amended By: EN 60601-2-37:2001/A1:2005 - Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
• Effective Date: 29-Jan-2023
• Amended By: EN 60601-2-37:2001/A2:2005 - Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
• Effective Date: 28-Jan-2023

Standards Content (Sample)

SLOVENSKI SIST EN 60601-2-37:2002
prva izdaja
STANDARD
junij 2002
Medical electrical equipment - Part 2-37: Particular requirements for the safety of
ultrasonic medical diagnostic and monitoring equipment (IEC 60601-2-37:2001)
ICS 11.040.55; 17.140.50 Referenčna številka
©  Standard je založil in izdal Slovenski inštitut za standardizacijo. Razmnoževanje ali kopiranje celote ali delov tega dokumenta ni dovoljeno

EUROPEAN STANDARD EN 60601-2-37
NORME EUROPÉENNE
EUROPÄISCHE NORM October 2001
ICS 11.040.55; 17.140.50
English version
Medical electrical equipment
Part 2-37: Particular requirements for the safety of
ultrasonic medical diagnostic and monitoring equipment
(IEC 60601-2-37:2001)
Appareils électromédicaux Medizinische elektrische Geräte
Partie 2-37: Règles particulières de Teil 2-37: Besondere Festlegungen für
sécurité pour les appareils de diagnostic die Sicherheit von Ultraschall-Geräten
et de surveillance médicaux à ultrasons für die medizinische Diagnose und
(CEI 60601-2-37:2001) Überwachung
(IEC 60601-2-37:2001)
This European Standard was approved by CENELEC on 2001-09-25. CENELEC members are bound to
comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European
Standard the status of a national standard without any alteration.
Up-to-date lists and bibliographical references concerning such national standards may be obtained on
application to the Central Secretariat or to any CENELEC member.
This European Standard exists in three official versions (English, French, German). A version in any other
language made by translation under the responsibility of a CENELEC member into its own language and
notified to the Central Secretariat has the same status as the official versions.
CENELEC members are the national electrotechnical committees of Austria, Belgium, Czech Republic,
Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Luxembo
...