BEUDAMED
    12 results · 28ms · Sources: EU EUDAMED, US FDA

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    MICROBAR MONITORING LINE FILTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SpineWand

    FDA UDI
    MORGAN STEER ORTHOPAEDICS LIMITED·05060696460019·Perc DLG Convenience Pack inc 17 gauge 8” Crawf...

    Coblation

    FDA UDI
    Smith & Nephew, Inc.·00817470004489·PERC DLG

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707067504·LIGATING MODULES 1 mm TRANSPARENT

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198734·AK3 Ultra Insert Trial Size 5, 10mm

    DIAFIL & DIAFIL Capsule

    FDA 510(k)
    FDA Class 2 ·Dental

    FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODELS KD-7901, KD-7905, KD-7911

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WALLSTENT RP ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code JCT·March 21, 2025

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 16, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·December 31, 2013

    BRILLIANT S+ VDD

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2010

    WALLSTENT? RP ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 21, 2025