BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Omni Legend

    FDA 510(k)
    FDA Class 2 ·Radiology

    MITEK, 30MM INTRAFIX TIBIAL SHEATH

    FDA Adverse Event
    Injury ·MITEK WORLDWIDE·Product code MBI·August 22, 2002

    SYNTHES 6.5 MM CANNULATED SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEM-7200-Z (BP742)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROXIMATE ILS CURVED CIR STAPL

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 5, 2008

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON INC·Product code GAM·August 24, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·July 5, 2013