BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    EBI XFIX DYNAFIX SYSTEM HA COATED SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPTI-PLAST 7F PERIPHERAL ANGIOPLASTY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ion Endoluminal System

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

    MENTOR SMOOTH ROUND HIGH PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·September 18, 2024

    UNIVERSAL DRIVER SHAFT

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·March 7, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    EVERA XT VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014

    MENTOR SMOOTH ROUND HIGH PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·August 14, 2024