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.

    DENTAURUM WIRES

    FDA 510(k)
    FDA Class 1 ·Dental

    SYNELISA U1-SNRNP (68KDA)-ANTIBODIES

    FDA 510(k)
    FDA Class 2 ·Immunology

    AMCATH DISPOSABLE BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RDIESSE DERMAL FILLER

    FDA Adverse Event
    Injury ·MERZ AESTHETICS INC.·Product code LMH·January 24, 2013

    REMB ELECTRIC WIREDRIVER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·December 6, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 3, 2014