BEUDAMED
    6 results · 19ms · 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 Regulation: Us FDA ×

    BAHADIR STERILIZATION CONTAINERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    REPROCESSED LIGASURE BLUNT TIP LAPAROSCOPIC SEALER/DIVIDER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 2, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 6, 2014

    SELF CENT HIP 40X28 RUST

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·July 18, 2013