BS-EN-ISO-18113-1 › Historical Revision Information
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Terms, definitions and general requirements
Document Center Inc. is an authorized dealer of BSI standards.
The following bibliographic material is provided to assist you with your purchasing decision:
The following bibliographic material is provided to assist you with your purchasing decision:
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)
Keywords
Clinical laboratory equipment;Instructions for use;Diagnosis (medical);Reagent solutions;Labelling (process);Clinical investigation instruments;Measurement;Labels;Medical equipment;Product information;Diagnostic reagents;Definitions
To find similar documents by classification:
11.100.10 (In vitro diagnostic test systems)
This document comes with our free Notification Service, good for the life of the document.
This document is available in either Paper or PDF format.
Document Number
BS EN ISO 18113-1:2009
Revision Level
2009 EDITION
Status
Superseded
Publication Date
Feb. 28, 2010
Replaced By
BS EN ISO 18113-1:2011
Page Count
60
ISBN
9780580565892
International Equivalent
ISO 18113-1:2009;EN ISO 18113-1:2009
Committee Number
CH/212