BEUDAMED
    14 results · 19ms · Sources: EU EUDAMED, US FDA

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    SAS SALMONELLA 0 FACTOR 8 ANTISERUM AND/OR SAS SALMONELLA 0 GROUP C2 FACTOR 9 ANTISERUM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    HA Bone Screws

    FDA UDI
    ORTHOFIX SRL·18032568861815·OSTEOTITE BONE SCREW 120/30 MM SHAFT D 6MM THRE...

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

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

    Adhesive Electrodes

    FDA 510(k)
    FDA Class 2 ·Neurology

    SYNTHES (USA) CRANIOMAXILLOFACIAL DISTRACTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    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