BEUDAMED
    323 results · 42ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    TYSHAK II CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·June 14, 2010

    COVERED CP STENT

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code PNF·December 15, 2016

    TYSHAK II

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code DQY·July 13, 2015

    TYSHAK MINI

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code DQY·October 25, 2017

    Z-MED II-X CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code DQY·November 21, 2017

    TYSHAK II

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code DQY·October 6, 2014

    TYSHAK II

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code DQY·November 26, 2014

    TYSHAK II CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·June 20, 2012

    Z-MED II CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·April 2, 2012

    BIB CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·January 3, 2002

    PTS CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·February 9, 2012

    IMPACT CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·January 19, 2012

    TYSHAK II

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code DQY·September 11, 2015

    TYSHAK II

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code DQY·August 6, 2015

    TYSHAK DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·July 27, 2000

    TYSHAK DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·July 27, 2000

    TYSHAK DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·July 27, 2000

    TYSHAK DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·July 27, 2000

    BIB CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·September 9, 2004

    MULLINS CATHETER

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code LIT·August 23, 2004