BEUDAMED
    8 results · 30ms · 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 ×

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 7, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 7, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 7, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 8, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 8, 2024

    ATLAS PLUS HF CRT-D

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC., CRMD·Product code NIK·June 18, 2014

    VANGUARD CR FEMORAL 60MM RIGHT INTERLOK

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code JWH·October 25, 2010

    MENISCAL CINCH, CURVED TIP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GAT·December 20, 2012