BEUDAMED
    7 results · 15ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Injury ×

    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

    CARPENTIER-EDWARDS PERIMOUNT AORTIC PERICARDIAL BIOPROSTHESIS

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

    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