BEUDAMED
    3 results · 15ms · 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 Status: Injury ×

    GUIDEWIRE, 1.6X150MM, CAPITAL FRAG

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code LXH·May 10, 2023

    GUIDEWIRE, 1.4MM, 3.5MM BEVELED FT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code LXH·May 10, 2023

    JUVEDERM (VOLUME/CONCENTRATION UNK)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·May 29, 2014