BEUDAMED
    6 results · 31ms · 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 XC

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

    AUTOSOFT XC

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

    AUTOSOFT XC

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

    TI COLLAR FOR 6MM DUAL-OPENING IMPLANTS

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·June 18, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·December 20, 2012

    POLYAXIAL HEAD 2 (PH2), UNKNOWN SIZE ROD

    FDA Adverse Event
    Malfunction ·THEKEN SPINE·Product code MNI·October 12, 2010