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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

01-12-2013

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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