BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    IMPLEX CEMENT RESTRICTOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    KENAFLEXX

    FDA UDI
    KENTRON HEALTHCARE, INC.·00852244007099·I.V. EXTENSION SET WITH KEN_SEF CONNECTOR 7.3" ...

    DREW SCIENTIFIC LTD. GLYCATED HAEMOGLOBIN TWO LEVEL CALIBRATOR KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AQUARIUS Gastrostomy Replacement Tube

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code KWA·February 5, 2013

    ARTICULEZE M HEAD 36MM +12

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·July 18, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 1, 2011