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SIST EN 60601-2-37:2002

(Main)

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

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Withdrawn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
31-May-2002
Withdrawal Date
21-Feb-2008
ICS
11.040.55 - Diagnostic equipment
17.140.50 - Electroacoustics
Technical Committee
IEMO - Electrical equipment in medical practice
Current Stage
9900 - Withdrawal (Adopted Project)
Start Date
14-Feb-2008
Due Date
08-Mar-2008
Completion Date
22-Feb-2008
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
Ref Project
EN 60601-2-37:2001 - Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment

Relations

Official Journal Project Relation
SIST 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
18-May-2009
Amended By
SIST EN 60601-2-37:2002/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
SIST EN 60601-2-37:2002/A2:2006 - Medical electrical equipment -- Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Effective Date
28-Jan-2023
Replaced By
SIST 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
SIST EN 60601-2-37:2002/A2:2006 - Medical electrical equipment -- Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Effective Date
07-Jun-2022
Amended By
SIST EN 60601-2-37:2002/A1:2005 - Medical electrical equipment -- Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Effective Date
07-Jun-2022
Replaced By
SIST 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
01-Apr-2008
Amended By
SIST EN 60601-2-37:2002/A2:2006 - Medical electrical equipment -- Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Effective Date
01-Mar-2006
Amended By
SIST EN 60601-2-37:2002/A1:2005 - Medical electrical equipment -- Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Effective Date
01-Jun-2005

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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
SIST EN 60601-2-37:2002(en)
©  Standard je založil in izdal Slovenski inštitut za standardizacijo. Razmnoževanje ali kopiranje celote ali delov tega dokumenta ni dovoljeno

---------------------- Page: 1 ----------------------

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
...

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