DS/ISO 18113-1:2022
Current
Current
The latest, up-to-date edition.
In vitro diagnostic medical devices– Information supplied by the manufacturer (labelling)– Part1:Terms, definitions, and general requirements
Published date
18-06-2024
Publisher
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This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.
| Committee |
DS/S-260
|
| DocumentType |
Standard
|
| PublisherName |
Danish Standards
|
| Status |
Current
|
| Standards | Relationship |
| ISO 18113-1:2022 | Identical |
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