PN EN ISO 18113-2 : 2011
Current
Current
The latest, up-to-date edition.
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
12-01-2013
Publisher
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Describes requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for professional use.
| Committee |
TC 300
|
| DevelopmentNote |
Supersedes PN EN 375. (03/2010) Polish translation issued on 22/11/2013. (01/2014)
|
| DocumentType |
Standard
|
| PublisherName |
Polish Committee for Standardization
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| ISO 18113-2:2009 | Identical |
| EN ISO 18113-2:2011 | Identical |
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