ÖNORM EN ISO 18113-1:2024 10 01
Current
Current
The latest, up-to-date edition.
In vitro diagnostic medical devices - Provision of information by the manufacturer (marking) - Part 1: Terms and general requirements (ISO 18113-1:2022)
Available format(s)
Hardcopy
Language(s)
German - English
Published date
01-10-2024
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 the information provided by the manufacturer of in vitro diagnostic medical devices.
| Committee |
ISO/TC 212
|
| DocumentType |
Standard
|
| Pages |
73
|
| ProductNote |
This standard also identical to EN ISO 18113-1:2022
|
| PublisherName |
Osterreichisches Normungsinstitut/Austrian Standards
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| EN ISO 18113-1:2024 | Identical |
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