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

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    Filters Regulation: Us FDA ×

    TunneLoc Tibial Fixation Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MORIA

    FDA UDI
    MORIA SA·03700483608300·

    ZIMMER CONTOUR PROVISIONAL COPING

    FDA 510(k)
    FDA Class 2 ·Dental

    ODYSSEY WORKSTATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·October 6, 2008

    UPHOLD VAGINAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 27, 2013

    PLUM XLM W/MODIFD B

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 22, 2011

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 14, 2023