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.

    DISPOSABLE HEMOSTAT (STRAIGHT&CURVED

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

    IMMULITE 2000 ACTH CALIBRATION VERIFICATION MATERIAL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PRESSURE WIRE SENSOR, MODELS 12004/12304

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 14, 2012

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code FZP·August 16, 2007

    CARELINK SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWS·June 10, 2015