BEUDAMED
    12 results · 30ms · Sources: EU EUDAMED, US FDA

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    MCSEER/MICRO CONTROLLER SLD ST EEG EVENT RECORDER

    FDA 510(k)
    FDA Class 2 ·Neurology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756348980·ABDOMINAL PACK

    MEDISYSTEMS LUER ACCESS INJECTION SITE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Enbio S

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 12, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 12, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 12, 2024

    ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

    FDA Adverse Event
    Injury ·COOK, INC.·Product code MIH·November 23, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 2, 2014

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·December 19, 2012

    TITANIUM NEXGEN LCCL FEMORAL SZ C-LT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 21, 2018

    NEXGEN LEGACY POSTERIOR STABILIZED ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 16, 2016