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TSE - TS EN ISO 18113-4

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4: 2009)

active, Most Current
Organization: TSE
Publication Date: 14 November 2014
Status: active
ICS Code (In vitro diagnostic test systems): 11.100.10
scope:

ISO 18113?un bu bolumu, kendi kendine test yapmak icin IVDreaktiflerinin imalatcisi tarafindan tedarik edilen bilgi icingerekleri kapsar. ISO 18113?un bu bolumu, kendi kendine test yapmakicin IVD tibbi cihazlarla birlikte kullanilmasi amaclanankalibratorler ve kontrol malzemeleri ile birlikte imalatcitarafindan tedarik edilen bilgilere de uygulanir. ISO 18113?un bubolumu, ayni zamanda aksesuarlara da uygulanabilir. ISO 18113?un bubolumu, dis ve ilk kaplardaki etiketlere ve kullanma talimatinauygulanir.

Document History

TS EN ISO 18113-4
November 14, 2014
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4: 2009)
ISO 18113?un bu bolumu, kendi kendine test yapmak icin IVDreaktiflerinin imalatcisi tarafindan tedarik edilen bilgi icingerekleri kapsar. ISO 18113?un bu bolumu, kendi kendine test yapmakicin IVD...
March 8, 2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing
A description is not available for this item.
March 23, 2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for selftesting
A description is not available for this item.
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