BEUDAMED
    3 results · 28ms · 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 ×

    10FR CORFLO ULTRA NASOGASTRIC TUBE

    FDA Adverse Event
    Malfunction ·CORPAK MEDSYSTEMS·Product code KNT·April 29, 2014

    ROD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·November 6, 2012

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 LARGE TITANIUM LIGATING CL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code FZP·September 20, 2007