BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    TYMPANOSTOMY TUBE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    OTI ORTHOPEDIC WIRE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    E-Z-EM PULSED INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PLMA DVC V11.51 1 N

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 12, 2014

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·February 11, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 10, 2011

    VIDAS ESTRADIOL II

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code CHP·January 21, 2021

    VIDAS® ESTRADIOL II

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code CHP·September 16, 2021