BEUDAMED
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    OMNIFIT CERAMIC MORSE TAPER HEAD (1002 SERIES)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3M™ Forsus™

    FDA UDI
    3M UNITEK CORPORATION·00652221110374·Forsus(TM) Fatigue Resistant Device Push Rod Me...

    MONARK 869 ERGOMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMMPULSE COATED TUBE PHENYTOIN ASSAY REAGENTS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PENUMBRA SYSTEM SEPARATOR 032

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·June 19, 2014

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·October 20, 2010

    MESH- COMPOSIX KUGEL

    FDA Adverse Event
    Injury ·DAVOL INC·Product code FTL·December 12, 2012