BEUDAMED
    1,423 results · 24ms · Sources: EU EUDAMED, US FDA

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    GORE EMBOLIC FILTER

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NTE·March 9, 2012

    GORE EMBOLIC FILTER

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCAITES·Product code NTE·January 10, 2013

    EFFICIA DFM100 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC·Product code MKJ·October 12, 2021

    GORE EMBOLIC FILTER

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NTE·November 21, 2012

    TRIAGE SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·December 22, 2023

    GORE EMBOLIC FILTER

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NTE·December 26, 2012

    SP, Ø 3.3MM RN, SLACT. 8MM, TIZR, GEF.

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·September 13, 2019

    S, Ø 3.3MM RN, SLACT. 10MM, TIZR, GEF.

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·September 13, 2019

    SP, Ø 3.3MM RN, SLACT. 10MM, TIZR, GEF.

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·September 16, 2019

    GORE EMBOLIC FILTER

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES,INC·Product code NTE·December 26, 2013

    SYRINGE 50ML LL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·December 29, 2024

    DERMAHOOK 1/2 HOOK

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GEF·August 14, 2015

    AUTO ENDO5 ML

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GEF·July 2, 2015

    MENISCAL APPLIER, OMNISPAN

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code GEF·September 21, 2015

    HOC PLUS ENDOTOUCH APPL 13" CVD

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GEF·July 13, 2015

    HOL L 10MM ENDO APPLIER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GEF·July 14, 2015

    OMNISPAN MENISCAL APPLIER

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code GEF·August 4, 2015

    MITEK ARTHROSCOPIC EQUIPMENT

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code GEF·March 15, 2012

    MITEK CORD CUTTER

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code GEF·April 25, 2014

    MITEK OMNISPAN MENISCAL APPLIER

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code GEF·April 21, 2014