BEUDAMED
    42 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    POLYETHER URETHANE MATERIAL CHANGE IN NEUROSTIMULATION LEADS

    FDA 510(k)
    FDA Class 2 ·Neurology

    ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HDL CHOLESTEROL PLUS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    EXCELSIOR MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code DQY·April 13, 2010

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIV.·Product code DQY·July 10, 2009

    EXCELSIOR SL-10 PRE-SHAPED 45 CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQO·December 12, 2007

    EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIV·Product code DQO·April 25, 2007

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQO·November 14, 2007

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORPORATION·Product code DQO·May 1, 2007

    EXCELSIOR SL-10 PRE-SHAPED CATHETER

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQO·September 14, 2006

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIV OF BOSTON SCIENTIFIC CORP·Product code DQO·January 3, 2007

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQO·September 15, 2006