BEUDAMED
    28 results · 23ms · Sources: EU EUDAMED, US FDA

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    V*CARE MANUAL RESUSCITATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GC Initial™

    FDA UDI
    Gc America Inc.·14548161315616·GC Initial™ LiSi Press Ingot LT-A4

    GC Initial™

    FDA UDI
    Gc America Inc.·D0470128421·GC Initial™ LiSi Press Ingot LT-A4

    EYE SENTIAL

    FDA UDI
    FGX INTERNATIONAL INC.·00193033444443·

    DRILL 1.5X105MM 22MM STP J-NT

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HBE·June 16, 2021

    DRILL 1.5X105MM 22MM STP J-NT

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HBE·April 28, 2021

    DRILL 1.5X105MM 22MM STP J-NT

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HBE·June 4, 2021

    SABRE COMPAC

    FDA 510(k)
    FDA Class 2 ·Neurology

    KINETIC CANNULA

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

    CONTACT DETACH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 13, 2025

    CONTACT DETACH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 22, 2025

    CONTACT DETACH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 11, 2025

    CONTACT DETACH

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 11, 2025

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 27, 2017

    23 G X .75 IN. BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 27, 2017

    MOVATION KNEE INSTRUMENT

    FDA Adverse Event
    ENCORE MEDICAL, L.P.·Product code LPH·March 20, 2013

    DELTA CER HEAD 12/14 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·February 24, 2011

    D-TRONPLUS POWER PACK

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·March 11, 2008

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR CLONMEL·Product code NIQ·August 13, 2010

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR CLONMEL·Product code NIQ·August 13, 2010