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.

    PEN, MARK-3 SKIN MARKING FOUNTAIN

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

    DENJECTOR

    FDA 510(k)
    FDA Class 2 ·Dental

    FlowTriever Retrieval/Aspiration System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·April 30, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 26, 2007

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·October 11, 2012