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

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    HOOK, IRIS, HERSHMAN

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209133963·

    QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SC

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ICONIX TT All Suture Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 28, 2014

    MBT CEM KEEL TIB TRAY SZ3

    FDA Adverse Event
    Injury ·DEPUY IRELAND·Product code NJL·October 3, 2012

    DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·May 13, 2015