BEUDAMED
    6 results · 33ms · Sources: EU EUDAMED, US FDA

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    FEMALE CONTINENCE DEVICE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MODIFICATION TO ZENIEVA

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

    FLOW-PAC LDH REAGENT SET

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    8F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·June 6, 2014

    PIROUET

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 27, 2010

    ASR ACETABULAR IMPLANT 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 21, 2012