EN ISO 18113-3:2009
Withdrawn
Withdrawn
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
Published date
12-15-2009
Publisher
Withdrawn date
12-31-2012
Sorry this product is not available in your region.
ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use.ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD instruments for professional use.ISO 18113-3:2009 can also be applied to accessories, where appropriate.
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Withdrawn
|
| Standards | Relationship |
| I.S. EN ISO 18113-3:2009 | Equivalent |
| BS EN ISO 18113-3:2009 | Equivalent |
| UNE-EN ISO 18113-3:2010 | Identical |
| BS EN ISO 18113-3:2009 | Identical |
Summarise
Sorry this product is not available in your region.