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

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    SLEEP-IN BONE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972023·posteriors; shade A3; size L; lower jaw

    ELLIPSE JUVIA, MODEL 9EJU7465

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CELFIRM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    TI TITAMAX IMPLANT (4.1)3.75X13 MM

    FDA Adverse Event
    Malfunction ·Product code DZE·July 14, 2015

    12.5FX24CM HEMO-CATH

    FDA Adverse Event
    Malfunction ·MEDCOMP·Product code MSD·February 15, 2013

    014 HT WINN GUIDE WIRE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code DQX·January 27, 2011

    5.0MM FLEXIBLE SHAFT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·March 27, 2024

    5.0MM FLEXIBLE SHAFT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·March 29, 2022

    HAMILTON MEDICAL AG

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·December 21, 2023