EN ISO 18113-1:2009
Withdrawn
Withdrawn
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
Published date
12-15-2009
Publisher
Withdrawn date
12-31-2012
Sorry this product is not available in your region.
ISO 18113-1:2009 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) medical devices.
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Withdrawn
|
| Standards | Relationship |
| I.S. EN ISO 18113-1:2009 | Equivalent |
| BS EN ISO 18113-1:2009 | Equivalent |
| BS EN ISO 18113-1:2009 | Identical |
| UNE-EN ISO 18113-1:2010 | Identical |
Summarise
Sorry this product is not available in your region.