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

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    STRYKER 1990 LIBERTY ELECTRIC CRITICAL CARE BED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRU-COLOR

    FDA 510(k)
    FDA Class 2 ·Dental

    PERCUTANEOUS ANGIOGRAPHIC NEEDLES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 30, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 30, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 30, 2024

    DENALI

    FDA Adverse Event
    Injury ·K2M, INC.·Product code MNH·June 16, 2014

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 19, 2010

    ENTERALITE INFINITY 500

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP (ZEVEX)·Product code FRN·November 12, 2012

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021