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.

    WR3500 AND WR3600 SERIES RECORDERS

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    PERIMETER THORACIC CATHETER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    AMSCO POLARIS SL

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

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 25, 2014

    TALENT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·November 5, 2010

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·December 20, 2012