BEUDAMED
    10 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Hepatic VCAR

    FDA 510(k)
    FDA Class 2 ·Radiology

    CHIMAERA HIP FRACTURE SYSTEM

    FDA UDI
    ORTHOFIX SRL·18054242515647·LAG SCREW COMPRESSION ROD

    MRI SYTEMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACCULIF TL-PEEK CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUANTUM MAVERICK MR BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·October 7, 2008

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 27, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·July 13, 2011

    LAG SCREWDRIVER

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code HSB·November 30, 2017

    LAG SCREW COMPRESSION ROD

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code HSB·November 30, 2017

    CHIMAERA HFS LAG SCREW SLIDING L90MM STERILE

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code HSB·November 30, 2017