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

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    ZIRCONIUM ALLOY UNI-POLAR HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CARDIOMATIC MODEL MSC-2001

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OK FLASH STERILIZATION INDICATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·July 16, 2014

    V18 CONTROL WIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP·Product code DQX·March 16, 2007

    V18 CONTROL WIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·May 23, 2007

    AJUST ADJUSTABLE SINGLE INCISION SLING

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code PAH·January 28, 2013

    ADVANCE(R) II MEDIAL-PIVOT TIBIAL INSERT

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JWH·December 21, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 4, 2014

    ECHOTIP ULTRA ULTRASOUND ASPIRATION NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·November 19, 2010

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·July 29, 2014

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·September 17, 2014