SS-EN ISO 18113-2:2024
Current
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022, IDT)
Hardcopy
English
09-02-2024
This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents, calibrators and controls intended for professional use.
| Committee |
ISO/TC 212
|
| DocumentType |
Standard
|
| Pages |
28
|
| PublisherName |
Standardiserings-Kommissionen I Sverige
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| ISO 18113-2:2022 | Identical |
| EN ISO 18113-2:2024 | Identical |
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