BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    CHYMOFAST TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    LONESTAR

    FDA UDI
    Orthofix US LLC·18257200090297·DIA 3.6MM PRIMARY BONE SCREW - 18MM

    INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TSX-101A/A AND TSX-101A/C AQUILION MULTISLICE CT SCANNERS

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNKNOWN URETEX MESH PRODUCT

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·May 19, 2014

    SHILEY

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code JOH·October 26, 2012

    CADD LEGACY PLUS

    FDA Adverse Event
    SMITHS MEDICAL·Product code FRN·August 22, 2010

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015