DS/EN ISO 18113-1:2024
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 (ISO 18113-1:2022)
Published date
19-06-2024
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
|
Supersedes |
Standards | Relationship |
EN ISO 18113-1:2024 | Identical |
ISO 18113-1:2022 | Identical |
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