TSE - TS EN ISO 18113-2
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
active, Most Current
| Organization: | TSE |
| Publication Date: | 12 November 2014 |
| Status: | active |
| ICS Code (In vitro diagnostic test systems): | 11.100.10 |
scope:
ISO 18113?un bu bolumu, profesyonel kullanim icin IVDreaktiflerinin imalatcisi tarafindan tedarik edilen bilgi icingerekleri kapsar.
Document History
TS EN ISO 18113-2
November 12, 2014
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
ISO 18113?un bu bolumu, profesyonel kullanim icin IVDreaktiflerinin imalatcisi tarafindan tedarik edilen bilgi icingerekleri kapsar.
March 8, 2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
A description is not available for this item.
March 23, 2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
A description is not available for this item.