BEUDAMED
    4 results · 35ms · 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 ×

    SPEC SILTEX RND 425CC

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·April 21, 2025

    OCCIPITAL-PL 4.5/5 MED W/50 TI

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code KWP·February 14, 2013

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 28, 2014

    UNKNOWN

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code N/A·January 7, 2011