BEUDAMED
    16 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code JXG·September 30, 2014

    PROGRAMMABLE VALVE SYSTEM SPECIAL DEVICE

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC./MEDOS S.A.·Product code JXG·August 14, 2006

    CODMAN LUMBER CATHETER KIT

    FDA Adverse Event
    Injury ·RAYNHAM·Product code JXG·March 9, 2023

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code JXG·July 28, 2014

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·December 30, 2013

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·June 19, 2013

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    CODMAN* LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·NATUS MEDICAL INCORPORATED·Product code JXG·April 28, 2021

    CODMAN EXT DRAINAGE SYSTEM III WITHOUT VENT CATH

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·April 4, 2016