BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    CHARNLEY FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RELIENT NAVIGATION DEVICE

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

    Gammex Cut-Resistant Glove Liner

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

    THRUWAY GUIDE WIRES

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·March 7, 2011

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES·Product code LZG·April 10, 2014

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 13, 2007

    M2A-MAGNUM PF CUP 52ODX46ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·September 26, 2012

    Heritage Labs Appraise A1c Diabetes Home Test , Product K7609, 24 kits/shipping carton (Product K7609), each kit packed in a box and contains 1 Triad Medium Alcohol Prep Pad, Cat. No. 10-3001, NDC 50730-3001-0, and blood specimen collection supplies, forms, and instructions Blood specimen collection

    FDA Recall
    Terminated ·Heritage Labs International LLC·Product code LCP·January 9, 2011