BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    5.0MM TITANIUM SCREW ANCHOR WITH NEEDLES

    FDA Adverse Event
    Malfunction ·BIOMET SPORTS MEDICINE·Product code HWC·October 11, 2016

    5.0MM TI W/ MAXBRAID NDLS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HWC·February 9, 2022

    5.0MM TI SCREW ANCHORS W/ MAXBRAID NEEDLES

    FDA Adverse Event
    Injury ·BIOMET SPORTS MEDICINE·Product code HWC·October 18, 2011

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 30, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 8, 2013

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·November 12, 2010

    5.0MM TI W/ MAXBRAID NDLS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HWC·February 9, 2022