BEUDAMED
    7 results · 22ms · 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.

    SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    TEMPUS PRO PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Endoscopy Irrigation Tubing

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

    LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·January 28, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·December 16, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 12, 2014

    CR TIBIAL INSERT SZ 2, 11MM, SLOPE ++

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 4, 2024