BEUDAMED
    6 results · 18ms · 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.

    PLASTIC FINGER CUFFS

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    EBERLE SHAVER SYSTEM C2 AND SHAVER BLADES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Bovie Bantam/PRO Electrosurgical Generator, Bovie DERM 941 Electrosurgical Generator, Bovie DERM 942 Electrosurgical Generator

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

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 19, 2007

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 26, 2012

    OMINIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·December 31, 2013