BEUDAMED
    345 results · 57ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    COLLATAPE

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES·Product code LPG·March 3, 2000

    MAYFIELD MODIFIED SKULL CLAMP

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code HBL·August 10, 2007

    ENDURA NO-REACT DURAL SUBSTITUTE, 4 CM X 4 CM

    FDA Adverse Event
    Injury ·SHELHIGH, INC.·Product code GXQ·November 14, 2007

    ENDURA NO-REACT DURAL SUBSTITUTE, 4 CM X 4 CM

    FDA Adverse Event
    Injury ·SHELHIGH·Product code GXQ·November 14, 2007

    ENDURA NO-REACT DURAL SUBSTITUTE, 4 CM X 4 CM

    FDA Adverse Event
    Injury ·SHELHIGH·Product code GXQ·November 14, 2007

    ENDURA NO-REACT SUBSTITUTE, 4 CM X 4 CM

    FDA Adverse Event
    Injury ·SHELHIGH INC.·Product code GXQ·November 14, 2007

    MAYFIELD TRIAD SKULL CLAMP

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·April 18, 2012

    MAQUET

    FDA Adverse Event
    Injury ·MAQUET GMBH AND CO. KG·Product code HBL·April 26, 2010

    MAQUET

    FDA Adverse Event
    Injury ·MAQUET GMBH & CO. KG·Product code HBL·April 26, 2010

    IDRT, UNKNOWN

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code MDD·July 13, 2022

    LUMBAR CATHETER ACCESSORY KIT (LCAK)

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES IMPLANTS S.A.·Product code JXG·December 5, 2007

    LUMBAR CATHETER ACCESSORY KIT(LCAK)

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES IMPLANTS S.A.·Product code JXG·December 5, 2007

    LUMBAR CATHETER ACCESSORY KIT (LCAK)

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES IMPLANTS S.A.·Product code JXG·December 5, 2007

    FLOWABLE WOUND MATRIX - UNSPECIFIED

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code KGN·January 4, 2019

    UNK

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES·Product code GXQ·November 27, 2007

    SURGIMEND MATRIX - UNSPECIFIED

    FDA Adverse Event
    Injury ·TEI BIOSCIENCES INC·Product code FTM·September 5, 2025

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·August 19, 2021

    SURGIMEND MATRIX - UNSPECIFIED

    FDA Adverse Event
    Injury ·TEI BIOSCIENCES INC·Product code FTM·January 3, 2019

    DURAGEN-UNKNOWN PRODUCT ID

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code GXQ·August 24, 2018

    DURAGEN RM DURAL REGENERATION MATRIX

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORP.·Product code GXQ·July 1, 2015