• There are no items in your cart
We noticed you’re not on the correct regional site. Switch to our AMERICAS site for the best experience.
Dismiss alert

PN EN ISO 18113-3 : 2011

Current

Current

The latest, up-to-date edition.

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

12-01-2013

Describes requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments for professional use.

Committee
TC 300
DevelopmentNote
Supersedes PN EN 591. (03/2010) Polish translation issued on 17/02/2015. (03/2015)
DocumentType
Standard
PublisherName
Polish Committee for Standardization
Status
Current
Supersedes

Standards Relationship
ISO 18113-3:2009 Identical
EN ISO 18113-3:2011 Identical

View more information
Sorry this product is not available in your region.

Access your standards online with a subscription

Features

  • Simple online access to standards, technical information and regulations.

  • Critical updates of standards and customisable alerts and notifications.

  • Multi-user online standards collection: secure, flexible and cost effective.