BEUDAMED
    6 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VANGUARD COMPLETE KNEE CRUCIATE RETAINING POROUS & HA FEMUR LEFT 75MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code MBH·December 16, 2016

    HOURGLASS

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code MQP·June 16, 2014

    SCR SFTSLK 2.0 PKG.8X20 STER

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code HWC·March 18, 2020

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 10, 2013

    C-LEG/C-LEG TUBE ADAPTER

    FDA Adverse Event
    Injury ·OTTO BOCK HEALTHCARE PRODUCTS GMBH·Product code ISW·June 10, 2008

    THE UNFOLDER® IMPLANTATION SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYB·April 16, 2011