BEUDAMED
    6 results · 22ms · 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 ×

    STRYKER SUCTION REGULATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SURGI-WRAP MAST TENDON SHEET

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

    Digital Automatic Blood Pressure Monitor BPM41 Series, Digital Automatic Blood Pressure Monitor BPM45 Series

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRIAL CABLE

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 16, 2014

    N/A

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code MSD·December 21, 2010

    ICAST COVERED STENT

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code JCT·January 2, 2013