BS-EN-ISO-18113-1 › Historical Revision Information
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Terms, definitions and general requirements
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In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)
Keywords
Definitions;Reagent solutions;Clinical laboratory equipment;Product information;Measurement;Labelling (process);Instructions for use;Clinical investigation instruments;Diagnostic reagents;Labels;Diagnosis (medical);Medical equipment
To find similar documents by classification:
11.100.10 (In vitro diagnostic test systems)
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Document Number
BS EN ISO 18113-1:2011
Revision Level
2011 EDITION
Status
Current
Publication Date
Jan. 31, 2012
Replaces
BS EN ISO 18113-1:2009
Page Count
62
ISBN
9780580773273
International Equivalent
EN ISO 18113-1:2011;ISO 18113-1:2009
Committee Number
CH/212