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

Superseded by EN 60601-2-37:2008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 (IEC 60601-2-37:2001/A2:2005)

General Information

• Status: Withdrawn
• Publication Date: 13-Dec-2005
• Withdrawal Date: 30-Nov-2008
• 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/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/A2:2006 - 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
• Amends: EN 60601-2-37:2001 - 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 STANDARD
01-marec-2006
0HGLFLQVNDHOHNWULþQDRSUHPDGHO3RVHEQHYDUQRVWQH]DKWHYH]D
XOWUD]YRþQRPHGLFLQVNRGLDJQRVWLþQRLQQDG]RURYDOQRRSUHPR,(&
$
Medical electrical equipment - Part 2-37: Particular requirements for the safety of
ultrasonic medical diagnostic and monitoring equipment (IEC 60601-2-37:2001/A2:2005)
Medizinische elektrische Geräte - Teil 2-37: Besondere Festlegungen für die Sicherheit
von Ultraschall-Geräten für die medizinische Diagnose und Überwachung (IEC 60601-2-
37:2001/A2:2005)
Appareils électromédicaux - Partie 2-37: Règles particulières de sécurité pour les
appareils de diagnostic et de surveillance médicaux à ultrasons (CEI 60601-2-
37:2001/A2:2005)
Ta slovenski standard je istoveten z: EN 60601-2-37:2001/A2:2005
ICS:
11.040.55
17.140.50
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EUROPEAN STANDARD EN 60601-2-37/A2
NORME EUROPÉENNE
EUROPÄISCHE NORM December 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/A2:2005)
Appareils électromédicaux Medizinische elektrische Geräte
Partie 2-37: Règles particulières Teil 2-37: Besondere Festlegungen für
de sécurité pour les appareils die Sicherheit von Ultraschall-Geräten für
de diagnostic et de surveillance médicaux die medizinische Diagnose und
à ultrasons Überwachung
(CEI 60601-2-37:2001/A2:2005) (IEC 60601-2-37:2001/A2:2005)

This amendment A2 modifies the European Standard EN 60601-2-37:2001; it was approved by
CENELEC on 2005-12-01. 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 nationa
...