BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OSTEOSITE STERILE SCREW, 120/30, 4.5/3.5 MM

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code HWC·April 1, 2008

    OSTEOTITE BONE SCREW 120/30 MM SHAFT D 6MM THREAD D 4.5-3.5MM

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDW·June 14, 2018

    OSTEOTITE BONE SCREW 120/30 MM SHAFT D 6MM THREAD D 4.5-3.5MM

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDW·June 14, 2018

    OSTEOTITE BONE SCREW 120/30 MM SHAFT D 6MM THREAD D 4.5-3.5MM

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDW·May 4, 2016

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·June 24, 2014

    CARPENTIER-EDWARDS PERIMOUNT AORTIC PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·February 13, 2013

    4 MOTOR ADVANCE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 17, 2010

    OSTEOTITE BONE SCREW 120/30 MM SHAFT D 6MM THREAD D 4.5-3.5MM

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDW·June 8, 2017

    OLIVE WIRE

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code KTT·June 8, 2017

    OSTEOTITE BONE SCREW 120/30 MM SHAFT D 6MM THREAD D 4.5-3.5MM

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDW·December 2, 2015