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

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    SYNTHES 1.3 MM SELF-DRILLING SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·April 14, 2015

    STRYKER PRESSURE MONITOR SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    CryoVizion System

    FDA 510(k)
    FDA Unclassified ·Unknown

    UNKNOWN DBS LEAD

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·February 28, 2013

    PINN LNR CON +4 NEUT 40IDX62OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWZ·January 31, 2011

    PROLENE POLYPROPYLENE MESH

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·August 6, 2014

    Veradius Unity with Software Release 2.1- Amobile, diagnostic X-ray imaging and viewing system. . Model Number: 718132

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 15, 2021