BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    RESUBMITTAL OF MI 1000C MICROIMAGER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACTIFUSE BONE GRAFT SUBSTITUTE AND E-Z-FIL AND SHAPE BONE GRAFT SUBSTITUTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Rusch FloCath Quick 18 Fr. Coudé Hydrophilic Intermittent Catheter

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWA·June 18, 2014

    VISISTAT SKIN STAPLER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDT·October 12, 2010

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON INC·Product code OTN·December 20, 2012

    INDUCTIGRAFT

    FDA Adverse Event
    Injury ·BAXTER APATECH LTD·Product code MQV·January 16, 2014

    INDUCTIGRAFT

    FDA Adverse Event
    Injury ·BAXTER APATECH LTD·Product code MQV·June 10, 2013

    INDUCTIGRAFT

    FDA Adverse Event
    Injury ·BAXTER APATECH LTD·Product code MQV·February 16, 2012