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

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    SUNGLASSES (NON-PRESCRIPTION)

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    GUIDE WIRE EXTENSION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ALARIS PUMP MODULE

    FDA Adverse Event
    Injury ·CAREFUSION CORP·Product code FRN·January 23, 2013

    PUMP MMT-722LCAB PRDGM INS BL EN LN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·December 6, 2010

    INTRAFIX TAPERED SCREW 7-9MM X 30MM (ACETAL/DELRIN)

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code MBI·July 15, 2014

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020