BEUDAMED
    7 results · 22ms · Sources: EU EUDAMED, US FDA

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    IMPLANTABLE PROGRAMMABLE CARDIAC PULSE GENERATORS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    CATHETER, CEBTRAL VENOUS, 2N1501

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

    CAPILLARYS Hb A1c

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 13, 2014

    MINI-CAP, DISCONNECT W/PVP-1SOLUTION

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·October 16, 2010

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·December 13, 2012

    ROCHE CARDIAC TROP T

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MMI·April 3, 2018