TSE - TS EN ISO 18113-1
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements(ISO 18113-1:2009)
active, Most Current
| Organization: | TSE |
| Publication Date: | 11 November 2014 |
| Status: | active |
| ICS Code (In vitro diagnostic test systems): | 11.100.10 |
scope:
ISO 18113?un bu bolumu, kavramlari tanimlar, genel ilkeleribelirler ve IVD tibbi cihazlarin imalatcilari tarafindan tedarikedilen bilgi icin temel gerekleri kapsar.
Document History
TS EN ISO 18113-1
November 11, 2014
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements(ISO 18113-1:2009)
ISO 18113?un bu bolumu, kavramlari tanimlar, genel ilkeleribelirler ve IVD tibbi cihazlarin imalatcilari tarafindan tedarikedilen bilgi icin temel gerekleri kapsar.
March 8, 2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
A description is not available for this item.
March 23, 2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
A description is not available for this item.