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.

    BIO CONDYLAR TM KNEE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACG-8511 PORTABLE ECG MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MULTIPLE (IZON DNA BLOOD COLLECTION KIT)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ADVANCE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·April 10, 2014

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·October 31, 2012

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·August 20, 2010