ISO 18113-1:2022
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
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
English, French
06-10-2022
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.
This document does not address language requirements since that is the domain of national laws and regulations.
This document does not apply to:
a) IVD medical devices for performance evaluation (e.g. for investigational use only);
b) shipping documents;
c) material safety data sheets / Safety Data Sheets;
d) marketing information (consistent with applicable legal requirements).
.
| DocumentType |
Standard
|
| Pages |
53
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| SS-EN ISO 18113-1:2024 | Identical |
| UNI EN ISO 18113-1:2024 | Identical |
| DS/ISO 18113-1:2022 | Identical |
| NF EN ISO 18113-1:2024 | Identical |
| DS/EN ISO 18113-1:2024 | Identical |
| SN EN ISO 18113-1:2024 | Identical |
| PNE-prEN ISO 18113-1 | Identical |
| CLSI EP34:2018(R2023) | Establishing and Verifying an Extended Measuring Interval Through Specimen Dilution and Spiking |
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