BEUDAMED
    4 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    BD INSTRUMENT MAX CLINICAL

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code OOI·September 21, 2020

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 25, 2013

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·March 11, 2011

    6.2MM TI CLICK'X PEDICLE SCR PREASSEMBLED

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code MNH·March 27, 2008