ISO 18113-5:2022
Current
The latest, up-to-date edition.
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing
Hardcopy , PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users
English, French
06-10-2022
This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments intended for self-testing.
This document is also applicable to apparatus and equipment intended to be used with IVD instruments for self-testing.
This document can also be applicable to accessories.
This document does not apply to:
a) instructions for instrument servicing or repair;
b) IVD reagents, including calibrators and control materials for use in control of the reagent;
c) IVD instruments for professional use.
| DocumentType |
Standard
|
| Pages |
10
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| NF EN ISO 18113-5:2024 | Identical |
| DS/EN ISO 18113-5:2024 | Identical |
| DS/ISO 18113-5:2022 | Identical |
| SS-EN ISO 18113-5:2024 | Identical |
| UNE-EN ISO 18113-5:2025 | Identical |
| BS EN ISO 18113-5:2024 | Identical |
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