BEUDAMED
    9 results · 32ms · Sources: EU EUDAMED, US FDA

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    DIFFERENTIATION DISKS PENICILLIN G 2 UNITS

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Boosting Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CLEARADEX GEL

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    7.0MM TI MATRIX REDUCTION SCREW 50MM THREAD LENGTH

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code NKB·August 24, 2015

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2014

    EVA BAG-500ML

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SAO PAULO·Product code BTC·October 7, 2010

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code MUZ·December 6, 2012

    7.0MM TI MATRIX REDUCTION SCREW 50MM THREAD LENGTH

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code NKB·September 8, 2015

    OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

    FDA Enforcement
    Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012