BS EN ISO 18113-3:2009 - In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for professional use

BS EN ISO 18113-3:2009

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for professional use

Status : Revised, Withdrawn   Published : February 2010 Replaced By : BS EN ISO 18113-3:2011

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Standard NumberBS EN ISO 18113-3:2009
TitleIn vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for professional use
StatusRevised, Withdrawn
Publication Date28 February 2010
Confirm Date05 August 2015
Withdrawn Date30 November 2011
Normative References(Required to achieve compliance to this standard)EN 980, ISO 14971, IEC 61010-2-101, ISO 15223-1, ISO 18113-1, IEC 62366, IEC 61326-2-6, IEC 61010-1
Informative References(Provided for Information)98/79/EC, ISO 18113-2, EN 591, ISO/IEC Directives Part 2
Replaced ByBS EN ISO 18113-3:2011
ReplacesBS EN 591:2001
International RelationshipsISO 18113-3:2009,EN ISO 18113-3:2009
Draft Superseded By06/30146518 DC
DescriptorsClinical investigation instruments, Medical equipment, Clinical laboratory equipment, Instructions for use, Labelling (process), Labels, Product information, Health service personnel, Diagnosis (medical)
ICS11.100.10
Title in FrenchDispositifs médicaux de diagnostic in vitro. Informations fournies par le fabricant (étiquetage). Instruments de diagnostic in vitro à usage professionnel
Title in GermanIn-vitro-Diagnostika. Bereitstellung von Informationen durch den Hersteller. Geräte für in-vitrodiagnostische Untersuchungen zum Gebrauch durch Fachpersonal
CommitteeCH/212
ISBN978 0 580 56591 5
PublisherBSI
FormatA4
DeliveryNo
Pages20
File Size410 KB
Price£130.00


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