BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    ELECTROMEDICS BLOOD HEAT EXCHANGER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MICRO FORCEPS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    CARDIOCAP II TM CH-RESP MONITORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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

    IN TOUCH ZU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 30, 2013

    PRECISION

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 24, 2010

    LASIK EYE SURGERY

    FDA Adverse Event
    Injury ·Product code LZS·July 10, 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