BEUDAMED
    4 results · 28ms · Sources: EU EUDAMED, US FDA

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    INDURA CATHETER

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code LKK·September 21, 2007

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 13, 2014

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 15, 2010

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·December 12, 2012