BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Arthrex Corkscrew and SwiveLock Suture Anchors

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Temporary Abutment

    FDA UDI
    BICON, LLC·00813110028747·4.0 x 4.5mm Scannable Temporary Abutment - 2.0m...

    BIOTENE MOISTURIZING MOUTH SPRAY FOR DRY MOUTH SYMPTOM RELIEF

    FDA 510(k)
    FDA Unclassified ·Unknown

    SP2 FEMORAL LOCKING NAIL, SP2 TIBIAL LOCKING NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD PEGASUS¿ SAFETY CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·December 16, 2019

    BD PEGASUS SAFETY CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·November 12, 2020

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·October 6, 2014

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 3, 2013

    SYNCHRON® SYSTEMS RHEUMATOID FACTOR (RF) REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·June 29, 2011