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.

    VENTRE/SPEC IGE CONTROLS

    FDA 510(k)
    FDA Class 2 ·Immunology

    ROSSMAX AUTOMATIC WRIST BLOOD PRESSURE MONITOR, MODELS B150 & Q400

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROGRIP LAPARSCOPIC SELF-FIXATING MESH

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

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 13, 2014

    MEDTRONIC INFUSE

    FDA Adverse Event
    Injury ·Product code NEK·October 31, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 3, 2015