Povučen
ISO 18113-4:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for self-testing.
ISO 18113-4:2009 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for self-testing.
ISO 18113-4:2009 can also be applied to accessories, where appropriate.
ISO 18113-4:2009 applies to the labels for outer and immediate containers and to the instructions for use.
POVUČEN
ISO 18113-4:2009
95.99
Povučen
6. 10. 2022.
OBJAVLJEN
ISO 18113-4:2022
Medicinska sredstva za dijagnostiku in vitro - Informacije izdate od strane proizvođača(obeležavanje) - Deo 4: Reagensi za dijagnostiku in vitro za samoispitivanje
95.99 Povučen
In vitro dijagnostička medicinska sredstva — Informacije izdate od strane proizvođača (obeležavanje) — Deo 4: Reagensi za dijagnostiku in vitro za samotestiranje
95.99 Povučen