BEUDAMED
    12 results · 44ms · Sources: EU EUDAMED, US FDA

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    INVIVO CORPORATION

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code DQA·May 12, 2010

    INVIVO CORPORATION

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code MWI·June 29, 2009

    INVIVO CORPORATION

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code MHX·July 27, 2009

    INVIVO CORPORATION PRECESS (3160 SERIES) MRI PATIENT MONITORING SYSTEM

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code MWI·March 24, 2011

    3160 MRI PATIENT MONITOR

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code MWI·February 3, 2010

    OMNI-TRAK

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code DRT·June 1, 2005

    4500 MRI PULSE OXIMETER

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code DQA·November 23, 2005

    NONE

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code DRT·October 31, 2005

    4500 MRI PULSE OXIMETER

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code DQA·October 13, 2005

    INVIVO/MDE ESCORT LINK CENTRAL STATION

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code DSI·October 18, 2011

    VISION CENTRAL STATION

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code DRT·August 18, 2005

    MODEL #800239

    FDA Adverse Event
    Other ·INVIVO CORPORATION·Product code MOS·September 11, 2006