BEUDAMED
    13 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.

    SPINETTE CENTRIFUGE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SternaFuse® Fixation System

    FDA UDI
    Fusion Innovations LLC·00810047770176·Variable Duo Base 2 Rings

    PLAYTEX EMBRACE PETITE BREAST PUMP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    InnoSEAL Hemostatic Pad

    FDA 510(k)
    FDA Unclassified ·Unknown

    NexGen® Legacy® Gender Solutions®

    FDA UDI
    Zimmer, Inc.·00889024191815·

    NexGen® Legacy® Gender Solutions®

    FDA UDI
    Zimmer, Inc.·00889024191853·

    NexGen® Legacy® Gender Solutions®

    FDA UDI
    Zimmer, Inc.·00889024191822·

    NexGen® Legacy® Gender Solutions®

    FDA UDI
    Zimmer, Inc.·00889024191860·

    NexGen® Legacy® Gender Solutions®

    FDA UDI
    Zimmer, Inc.·00889024191846·

    NexGen® Legacy® Gender Solutions®

    FDA UDI
    Zimmer, Inc.·00889024191839·

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 21, 2014

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 19, 2007

    ACCU-CHEK ® COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 26, 2012