BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    Pocket III

    FDA 510(k)
    FDA Class 2 ·Radiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517630582·CoRoent Ant TLIF Ti, 13x12x30mm 12°

    XIVE TG ABUTMENTS

    FDA 510(k)
    FDA Class 2 ·Dental

    QXLINK

    FDA 510(k)
    FDA Class 2 ·Radiology

    IMP,TSV,4.1MM,SBM,10

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·August 28, 2023

    IMP,TSV,4.1MM,SBM,10

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·November 3, 2021

    BREEZE2 TEST STRIPS

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·June 7, 2007

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 21, 2025

    MENTOR SMOOTH ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·September 2, 2020

    BREAS VIVO 50 FW2.00

    FDA Adverse Event
    Malfunction ·BREAS MEDICAL AB·Product code NOU·June 19, 2014

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·September 2, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 18, 2015