SS-EN ISO 18113-1 : 2011
Superseded
Superseded
View Superseded by
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
Published date
11-21-2011
Publisher
Superseded date
09-21-2024
Superseded by
Sorry this product is not available in your region.
This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.
| Committee |
TC 212
|
| DocumentType |
Standard
|
| ProductNote |
THIS STANDARD IS IDENTICAL WITH : EN ISO 18113-1 : 2011
|
| PublisherName |
Standardiserings-Kommissionen I Sverige
|
| Status |
Superseded
|
| SupersededBy |
| Standards | Relationship |
| ISO 18113-1:2009 | Identical |
Summarise
Sorry this product is not available in your region.