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

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    SENSOR AMPLIFIER

    FDA 510(k)
    FDA Class 2 ·Neurology

    EMBRACE GEL

    FDA 510(k)
    FDA Class 2 ·Radiology

    RESPIRATOR DISCONNECT ALARM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DATASCOPE MR MONITOR

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP./PT MONITORING DIVISION·Product code MHX·January 23, 2003

    ASSY, PROBE, BLADDERSCAN BVI 9400/9600

    FDA Adverse Event
    Malfunction ·VERATHON MEDICAL·Product code IYO·February 15, 2013

    EYE SURGERY STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FPO·December 30, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 1, 2014