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

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    Filters Regulation: Us FDA ×

    CORDIS TUNNELER

    FDA 510(k)
    FDA Class 1 ·Neurology

    SURGICAL STOCKINGS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RM Electrode (RMH 23-01)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ACCESS 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·December 17, 2010

    SPARC SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTN·January 25, 2013

    VERIFLEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·July 14, 2014