BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HYPODERMIC NEEDLE PRO SYRINGE AND NEEDLE WITH NEEDLE PROTECT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·September 25, 2006

    GORE® TRI-LOBE BALLOON CATHETER

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·February 26, 2016

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 13, 2014

    TOTAL ASR FEM IMP SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·December 7, 2012

    OT PING ENHANCED METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 23, 2015

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·February 26, 2016