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

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    DISPOSABLE FORCEPS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123120·K-WIRE - DOUBLE TROCAR 0.9mm DIA x 150mm

    ADULT SILICONE EAR PLUGS, MODELS # 68053, 68057

    FDA 510(k)
    FDA Unclassified ·Unknown

    CPS DIRECT MEDIGUIDE ENABLED OUTER CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 19, 2016

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 1, 2016

    SOLOIST SINGLE NEEDLE ELECTRODEELECTRODE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code GEI·December 10, 2010

    EXPRESS® LD BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·January 17, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 8, 2014

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·March 8, 2019