Povučen
ISO 18113-2:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for professional use.
ISO 18113-2:2009 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for professional use.
ISO 18113-2:2009 can also be applied to accessories.
ISO 18113-2:2009 applies to the labels for outer and immediate containers and to the instructions for use.
POVUČEN
ISO 18113-2:2009
95.99
Povučen
6. 10. 2022.
OBJAVLJEN
ISO 18113-2:2022
Medicinska sredstva za dijagnostiku in vitro - Informacije izdate od strane proizvođača (obeležavanje) - Deo 2: Reagensi za dijagnostiku in vitro za profesionalnu upotrebu
95.99 Povučen
In vitro dijagnostička medicinska sredstva — Informacije izdate od strane proizvođača (obeležavanje ) — Deo 2: In vitro dijagnostički reagensi za profesionalnu upotrebu
95.99 Povučen