BEUDAMED
    9 results · 17ms · 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.

    HERPTRAN CONCENTRATE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Lower Crown Pack for Herbst LL6 8mm

    FDA UDI
    SPECIALTY APPLIANCES, LLC·D8199007130·

    Mariner

    FDA UDI
    Seaspine Orthopedics Corporation·10889981129132·Counter Torque, Long

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221111043·3M™ Unitek™ Prestige Posterior Band Removing Pl...

    ELEVATE PROLAPSE REPAIR SYSTEM WITH PC COATED INTEPRO LITE- APICAL AND POSTERIOR PROLAPSE REPAIR SYSTEM, ANTERIOR AND AP

    FDA 510(k)
    FDA Class 3 ·Obstetrics/Gynecology

    EchoNavigator

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MPRI·Product code DTB·June 27, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 16, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 8, 2013