BEUDAMED
    8 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·December 18, 2014

    11.0MM TI HELICAL BLADE 115MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES ELMIRA·Product code HSB·August 22, 2017

    COMPLETE SE ILIAC

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIO·October 23, 2012

    GALILEO ECHO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·May 8, 2014

    UNKNOWN DEPUY STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·August 10, 2010

    11.0MM TI HELICAL BLADE 110MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES ELMIRA·Product code HSB·August 22, 2017

    11.0MM TI HELICAL BLADE 110MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES ELMIRA·Product code HSB·August 22, 2017

    MAYO SUPERCUT D-EDGES SCISSORS CVD 6-3/4

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code LRW·August 20, 2018