Search BSI Knowledge
Cookie Settings
Standard
Withdrawn
BS EN ISO 18113-1:2009
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) - Terms, definitions and general requirements
Published:
28 Feb 2010
•
Withdrawn:
31 Oct 2011
Overview
Preview
References
History
Visit the preview section for more information
Product Details
Descriptors
Clinical laboratory equipment
Instructions for use
Diagnosis (medical)
Reagent solutions
Labelling (process)
Clinical investigation instruments
Measurement
Labels
Medical equipment
Product information
Diagnostic reagents
Definitions
ICS Codes
11.100.10 In vitro diagnostic test systems
Committee
CH/212
International relationships
Identical to:
EN ISO 18113-1:2009
ISO 18113-1:2009
ISBN
978 0 580 56589 2
Publisher
BSI