BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    HWJECT Auto-disable syringe

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Deltec

    FDA UDI
    ICU MEDICAL, INC.·10610586025129·

    Insignia

    FDA UDI
    ALPHATEC SPINE, INC.·00190376264462·4.0mm Fixed Angle, Self Tapping Screw, Dual Lea...

    TESCERA FIBER BUNDLES, FIBER MESH AND FIBER CYLINDERS

    FDA 510(k)
    FDA Class 2 ·Dental

    SOFIA 88 Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 22, 2025

    DURA DURATION ALL POLY PAT LG

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code JWH·August 29, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 7, 2014

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 18, 2013

    9 Fr Introducer Set, REF 21-2340-24

    FDA Recall
    Terminated ·Deltec, Inc·Product code DYB·March 29, 2004