BEUDAMED
    72 results · 36ms · Sources: EU EUDAMED, US FDA

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    PUMP, CONTINUOUS WAVE III

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code HRX·July 1, 2008

    ANGIOJET AVX RHEOLYTIC THROMBECTOMY SET

    FDA Adverse Event
    Other ·BAYER INTERVENTIONAL INC·Product code DXE·March 16, 2012

    ANGIOJET AVX THROMBECTOMY CATHETER

    FDA Adverse Event
    Other ·BAYER INTERVENTIONAL, INC.·Product code DXE·October 25, 2012

    JETSTREAM NAVITUS

    FDA Adverse Event
    Other ·BAYER INTERVENTIONAL, INC·Product code MCW·June 13, 2012

    JETSTREAM NAVITUS L

    FDA Adverse Event
    Other ·BAYER INTERVENTIONAL INC·Product code MCW·June 1, 2012

    JETSTREAM NAVITUS

    FDA Adverse Event
    Other ·BAYER INTERVENTIONAL, INC·Product code MCW·June 6, 2012

    ANGIOJET AVX THROMBECTOMY CATHETER

    FDA Adverse Event
    Other ·BAYER INTERVENTIONAL INC·Product code DXE·June 1, 2012

    JETSTREAM G3 SF

    FDA Adverse Event
    Other ·BAYER INTERVENTIONAL, INC.·Product code MCW·June 21, 2012

    DVX THROMBECTOMY SET

    FDA Adverse Event
    Other ·BAYER INTERVENTIONAL, INC.·Product code DXE·June 8, 2012

    VULCAN GENERATOR

    FDA Adverse Event
    Other ·ORATEC INTERVENTIONS, INC.·Product code GEI·February 25, 2002

    VULCAN RF GENERATOR

    FDA Adverse Event
    Other ·ORATEC INTERVENTIONS, INC.·Product code GEI·February 25, 2002

    ANGIOJET XPEEDIOR RHEOLYLIC THROMBECTOMY SET

    FDA Adverse Event
    Other ·BAYER INTERVENTIONAL, INC.·Product code DXE·February 15, 2012

    SPINECATH INTRADISCAL CATHETER

    FDA Adverse Event
    Other ·ORATEC INTERVENTIONS, INC.·Product code GEI·August 15, 2000

    SPINECATH INTRADISCAL CATHETER

    FDA Adverse Event
    Other ·ORATEC INTERVENTIONS, INC.·Product code GEI·August 15, 2000

    VULCAN TAC-S ELECTROTHERMAL PROBE

    FDA Adverse Event
    Other ·ORATEC INTERVENTIONS, INC.·Product code GEI·August 15, 2000

    SPINECATH INTRADISCAL CATHETER

    FDA Adverse Event
    Other ·ORATEC INTERVENTIONS, INC.·Product code GEI·April 18, 2000

    SPINECATH INTRADISCAL CATHETER

    FDA Adverse Event
    Other ·ORATEC INTERVENTIONS, INC.·Product code GEI·June 22, 2000

    VULCAN GENERATOR

    FDA Adverse Event
    Other ·ORATEC INTERVENTIONS, INC.·Product code GEI·November 20, 2000

    ABLATOR-S 90 DEGREE

    FDA Adverse Event
    Other ·ORATEC INTERVENTIONS, INC.·Product code GEI·November 28, 2000

    PERPOS PLS

    FDA Adverse Event
    Other ·INTERVENTIONAL SPINE INC.·Product code MRW·February 28, 2011