BS 5724-2-2.11:1989, IEC 60601-2-11:1987 - Medical electrical equipment. Particular requirements for safety. Specification for gamma beam therapy equipment

BS 5724-2-2.11:1989, IEC 60601-2-11:1987

Medical electrical equipment. Particular requirements for safety. Specification for gamma beam therapy equipment

Status : Superseded, Withdrawn   Published : September 1989 Replaced By : BS EN 60601-2-11:1998, BS 5724-2.11:1998 IEC 60601-2-

WITHDRAWN TITLE
*To ask about withdrawn titles contact the
BSI Customer Services
cservices@bsigroup.com, +44 345 086 9001


Safety, design and construction of equipment for radiotherapy.




Standard NumberBS 5724-2-2.11:1989, IEC 60601-2-11:1987
TitleMedical electrical equipment. Particular requirements for safety. Specification for gamma beam therapy equipment
StatusSuperseded, Withdrawn
Publication Date29 September 1989
Confirm Date15 October 1996
Withdrawn Date15 April 1998
Normative References(Required to achieve compliance to this standard)No other standards are normatively referenced
Informative References(Provided for Information)No other standards are informatively referenced
Replaced ByBS EN 60601-2-11:1998, BS 5724-2.11:1998 IEC 60601-2-
International RelationshipsIEC 60601-2-11:1987
Amended ByAMD 6804
Draft Superseded By81/29347 DC
DescriptorsElectrical medical equipment, Medical equipment, Radiotherapy, Radiology apparatus (medical), Medical radiology, Gamma-ray apparatus, Safety measures, Marking, Documents, Instructions for use, Radiation protection, Environment (working), Definitions, Design, Graduations, Direction of movement
ICS11.040.50
13.280
Title in FrenchAppareils électromédicaux. Règles particulières de sécurité. Equipements de gammathérapie. Spécifications
Title in GermanElektromedizinische Geraete. Besondere Sicherheitsanforderungen. Gamma-Bestrahlungseinrichtungen
CommitteeCH/62/3
ISBN0 580 17495 6
PublisherBSI
FormatA4
DeliveryNo
Pages30
File Size680 KB
Price£182.00


WITHDRAWN TITLE
*To ask about withdrawn titles contact the
BSI Customer Services
cservices@bsigroup.com, +44 345 086 9001
 Your basket
Your basket is empty

Multi-user access to over 3,500 medical device standards, regulations, expert commentaries and other documents


Develop a PAS

Develop a fast-track standardization document in 9-12 months


Worldwide Standards
We can source any standard from anywhere in the world


Tracked Changes

Understand the changes made to a standard with our new Tracked Changes version