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21/30416029 DC | 11 Aug 2021 | BSI Knowledge
Standard
21/30416029 DC
BS EN ISO 18113-1. In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) - Part 1. Terms, definitions, and general requirements
Current
•
Published:
11 Aug 2021
Overview
Preview
References
History
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Product Details
Descriptors
Definitions
Reagent solutions
Clinical laboratory equipment
Product information
Measurement
Labelling (process)
Instructions for use
Clinical investigation instruments
Diagnostic reagents
Labels
Diagnosis (medical)
Medical equipment
ICS Codes
11.100.10 In vitro diagnostic test systems
Committee
CH/212
International relationships
Identical to:
ISO/DIS 18113-1
ISBN
—
Publisher
BSI