BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    AIA-PACK AFP CALIBRATION VERIFICATION TEST SET

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SUTTER MODEL 10000 LEG CPM DEVICE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    CONTROLLED PASSIVE MOTION MACHINE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    STE NAVICULAR PLT LT SMALL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRS·December 14, 2017

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 22, 2013

    HAKIM INLINE PROGRAMMABLE VALVE SG

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·December 9, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 5, 2014