BEUDAMED
    9 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    RESOLUTE ONYX RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·January 31, 2019

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·April 9, 2019

    ISTENT INJECT W TRABECULAR MICRO-BYPASS SYSTEM

    FDA Adverse Event
    Malfunction ·GLAUKOS CORPORATION·Product code OGO·January 13, 2020

    FOUNDATION SHOULDER

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code KWS·June 13, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011

    INNOVATOR POST-OPERATIVE KNEE BRACE

    FDA Adverse Event
    Injury ·OSSUR AMERICAS·Product code ITQ·March 11, 2008

    INTRAOCULAR PRESSURE LOWERING IMPLANT

    FDA Adverse Event
    Malfunction ·GLAUKOS CORPORATION·Product code OGO·January 29, 2020

    SOL-M 3 ML LUER LOCK SYRINGE W/O NEEDLE

    FDA Adverse Event
    Injury ·SOL-MILLENNIUM MEDICAL INC.·Product code FMF·November 21, 2020

    RESOLUTE ONYX RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·July 1, 2021