SIST EN 60601-2-50:2002

Medical electrical equipment -- Part 2-50: Particular requirements for the safety of infant phototherapy equipment

Specifies requirements applicable to infant phototherapy equipment which by means of visible radiation serve to reduce bilirubin in the body of infants suffering from icterus in the first months of life. Specifies tests for demonstrating compliance with these requirements.

Medizinische elektrische Geräte -- Teil 2-50: Besondere Festlegungen für die Sicherheit von Säuglings-Phototherapiegeräten

Appareils électromédicaux -- Partie 2-50: Prescriptions particulières de sécurité des appareils de photothérapie infantile

Medical electrical equipment - Part 2-50: Particular requirements for the safety of infant phototherapy equipment

General Information

• Status: Withdrawn
• Publication Date: 31-Aug-2002
• Withdrawal Date: 09-Jun-2009
• ICS: 11.040.60 - Therapy equipment
• Technical Committee: IEMO - Electrical equipment in medical practice
• Current Stage: 9900 - Withdrawal (Adopted Project)
• Start Date: 09-Jun-2009
• Due Date: 02-Jul-2009
• Completion Date: 10-Jun-2009
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Ref Project: EN 60601-2-50:2002 - Medical electrical equipment - Part 2-50: Particular requirements for the safety of infant phototherapy equipment

Relations

• Revised: SIST EN 60601-2-50:2009 - Medical electrical equipment - Part 2-50: Particular requirements for basic safety and essential performance of infant phototherapy equipment (IEC 60601-2-50:2009)
• Effective Date: 08-May-2012
• Replaced By: SIST EN 60601-2-50:2009 - Medical electrical equipment - Part 2-50: Particular requirements for basic safety and essential performance of infant phototherapy equipment (IEC 60601-2-50:2009)
• Effective Date: 28-Jan-2023
• Replaced By: SIST EN 60601-2-50:2009 - Medical electrical equipment - Part 2-50: Particular requirements for basic safety and essential performance of infant phototherapy equipment (IEC 60601-2-50:2009)
• Effective Date: 07-Jun-2022
• Replaced By: SIST EN 60601-2-50:2009 - Medical electrical equipment - Part 2-50: Particular requirements for basic safety and essential performance of infant phototherapy equipment (IEC 60601-2-50:2009)
• Effective Date: 01-Jul-2008

Standards Content (Sample)

SLOVENSKI SIST EN 60601-2-50:2002
prva izdaja
STANDARD
september 2002
Medical electrical equipment - Part 2-50: Particular requirements for the safety of
infant phototherapy equipment
ICS 11.040.60 Referenčna številka
SIST EN 60601-2-50:2002(en)
©  Standard je založil in izdal Slovenski inštitut za standardizacijo. Razmnoževanje ali kopiranje celote ali delov tega dokumenta ni dovoljeno

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EUROPEAN STANDARD EN 60601-2-50
NORME EUROPÉENNE
EUROPÄISCHE NORM February 2002
ICS 11.040.60
English version
Medical electrical equipment
Part 2-50: Particular requirements for the safety
of infant phototherapy equipment
(IEC 60601-2-50:2000 + corrigendum March 2001)
Appareils électromédicaux Medizinische elektrische Geräte
Partie 2-50: Prescriptions particulières Teil 2-50: Besondere Festlegungen
de sécurité des appareils de für die Sicherheit von Säuglings-
photothérapie infantile Phototherapiegeräten
(CEI 60601-2-50:2000 + (IEC 60601-2-50:2000 +
corrigendum mars 2001) Corrigendum März 2001)
This European Standard was approved by CENELEC on 2000-09-01. 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, Luxembourg, Malta, Netherlands,
Norway, Portugal, Spain, Sweden, Switzerland and United Kingdom.
CENELEC
European Committee for Electrotechnical Standardization
Comité Européen de Normalisation Electrotechnique
Europäisches Komitee für Elektrotechnische Normung
Central Secretariat: rue de Stassart 35, B - 1050 Brussels
© 2002 CENELEC - All rights of exploitation in any form and by any means reserved worldwide for CENELEC members.
Ref. No. EN 60601-2-50:2002 E

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EN 60601-2-50:2002 - 2 -
Foreword
The text of document 62D/363/FDIS, future edition 1 of IEC 60601-2-50, prepared by SC 62D,
Electromedical equipment, of IEC TC 62, Electrical equipment in medical practice, was submitted to
the IEC-CENELEC parallel vote and was approved by CENELEC as EN 60601-2-50 on 2000-09-01.
The following dates were fixed:
– latest date by which the EN has to be implemented
at national level by publication of an identical
national standard or by endorsement (dop) 2002-08-01
– latest date by which the national standards conflicting
with the EN have to be withdrawn (dow) 2003-09-01
Annexes designated "normative" are part of th
...