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SIST EN 60601-2-37:2002/A1:2005

(Amendment)

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

Superseded by EN 60601-2-37:2008

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

Medicinska električna oprema – 2-37. del: Posebne varnostne zahteve za ultrazvočno medicinsko diagnostično in nadzorovalno opremo

General Information

Status
Withdrawn
Publication Date
31-May-2005
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
Ref Project
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

Relations

Amends
SIST EN 60601-2-37:2002 - Medical electrical equipment -- Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Effective Date
01-Jun-2005
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
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
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
Amends
SIST EN 60601-2-37:2002 - Medical electrical equipment -- Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Effective Date
29-Jan-2023
Amends
SIST EN 60601-2-37:2002 - Medical electrical equipment -- Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Effective Date
07-Jun-2022

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EN 60601-2-37:2002/A1:2005
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Standards Content (Sample)

SLOVENSKI SIST EN 60601-2-
37:2002/A1:2005

STANDARD
junij 2005
Medicinska električna oprema – 2-37. del: Posebne varnostne zahteve za
ultrazvočno medicinsko diagnostično in nadzorovalno opremo
Medical electrical equipment - Part 2-37: Particular requirements for the safety of
ultrasonic medical diagnostic and monitoring equipment
ICS 11.040.55; 17.140.50 Referenčna številka
SIST EN 60601-2-37:2002/A1:2005(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/A1
NORME EUROPÉENNE
EUROPÄISCHE NORM February 2005

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/A1:2004)


Appareils électromédicaux Medizinische elektrische Geräte
Partie 2-37: Règles particulières Teil 2-37: Besondere Festlegungen
de sécurité pour les appareils für die Sicherheit von Ultraschall-Geräten
de diagnostic et de surveillance médicaux für die medizinische Diagnose
à ultrasons und Überwachung
(CEI 60601-2-37:2001/A1:2004) (IEC 60601-2-37:2001/A1:2004)






This amendment A1 modifies the European Standard EN 60601-2-37:2001; it was approved by
CENELEC on 2004-12-07. CENELEC members are bound to comply with the CEN/CENELEC Internal
Regulations which stipulate the conditions for giving this amendment 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 amendment exists in three official versions (English, French, German). A version in any other language
mad
...

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