IEC 60601-2-50:2000

IEC 60601-2-50:2000

July 2000
International standard Cancelled

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.The object of this Particular Standard is to establish requirements for infant phototherapy equipment which reduce the safety hazards to patients and operators as much as possible and to specify tests for demonstrating compliance with these requirements.

Main informations

Collections

International IEC standards

Publication date

July 2000

Number of pages

24 p.

Reference

IEC 60601-2-50:2000

Print number

1
Sumary
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. The object of this Particular Standard is to establish requirements for infant phototherapy equipment which reduce the safety hazards to patients and operators as much as possible and to specify tests for demonstrating compliance with these requirements.
Standard replaced by (1)
IEC 60601-2-50:2009
March 2009
International standard Cancelled
Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment

IEC 60601-2-50:2009 establishes particular basic safety and essential performance requirements for infant phototherapy equipment, which reduce the safety hazards to patients and operators as much as possible, and specifies tests for demonstrating compliance with these requirements. This second edition cancels and replaces the first edition published in 2000. This edition constitutes a technical revision. The main purpose of this new edition is to provide consistency with the third edition of the general standard. This edition further provides consistency with the four other particular standards related to pediatric equipment for which the committee is responsible. The contents of the corrigendum of August 2010 have been included in this copy.

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