SS-EN ISO 18113-1:2024
Current
Current
The latest, up-to-date edition.
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022, IDT)
Available format(s)
Hardcopy
Language(s)
English
Published date
02-09-2024
Publisher
Important note : Users cannot be edited or removed once added to your Multi user PDF.This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.
| Committee |
ISO/TC 212
|
| DocumentType |
Standard
|
| Pages |
68
|
| PublisherName |
Standardiserings-Kommissionen I Sverige
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| ISO 18113-1:2022 | Identical |
| EN ISO 18113-1:2024 | Identical |
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