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

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    Filters Regulation: Us FDA ×

    MODIFIED NEW JERSEY FEMORAL HIP RESURFACING COMPON

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEGUFILL (R) BOND

    FDA 510(k)
    FDA Class 2 ·Dental

    PATHODX CHLAMYDIA TRACHOMATIS DIRECT SPECIMEN TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    M2A-MAGNUM MODULAR HEAD SIZE 54MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 9, 2013

    HF KIT F.AQUARIUS W/HF12AQUAMAX FILTER

    FDA Adverse Event
    Malfunction ·HAEMOTRONICS SPA·Product code FJK·November 22, 2010

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 1, 2014

    BI-ANGULAR HUMERAL HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBF·March 23, 2017

    Pipeline Flex Embolization Device

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