EN ISO 18113-2:2011
Withdrawn
Withdrawn
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
Published date
10-19-2011
Publisher
Withdrawn date
10-31-2014
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ISO 18113-2:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for professional use.ISO 18113-2:2009 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for professional use.ISO 18113-2:2009 can also be applied to accessories.ISO 18113-2:2009 applies to the labels for outer and immediate containers and to the instructions for use.
| Committee |
CEN/TC 140
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Withdrawn
|
| Supersedes |
| Standards | Relationship |
| BS EN ISO 18113-2:2011 | Identical |
| NF EN ISO 18113-2 : 2012 | Identical |
| I.S. EN ISO 18113-2:2011 | Identical |
| NEN EN ISO 18113-2 : 2011 | Identical |
| DIN EN ISO 18113-2:2013-01 | Identical |
| PN EN ISO 18113-2 : 2011 | Identical |
| NS EN ISO 18113-2 : 2011 | Identical |
| NBN EN ISO 18113-2 : 2011 | Identical |
| ISO 18113-2:2009 | Identical |
| DS EN ISO 18113-2 : 2011 | Identical |
| UNE-EN ISO 18113-2:2012 | Identical |
Summarise
Sorry this product is not available in your region.