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

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    Filters FDA Adverse Event ×

    ROI-A INSET MEDIAN IMPLANT H14MM 27X36MM

    FDA Adverse Event
    Injury ·LDR MEDICAL·Product code OVD·November 13, 2019

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·June 8, 2013

    ASR UNI FEMORAL IMPL SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·May 12, 2011

    ACCU-THERM

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, INC.·Product code IMD·September 8, 2008

    SENTRANT INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC VASCULAR·Product code DYB·May 18, 2026

    ROI-A INSET MEDIAN IMPLANT H16MM 27X36MM 14

    FDA Adverse Event
    Malfunction ·LDR MÉDICAL·Product code MAX·April 23, 2019

    ROI-A INSET MEDIAN IMPLANT H16MM 30X39MM

    FDA Adverse Event
    Malfunction ·LDR MÉDICAL·Product code MAX·January 27, 2023

    ROI-A INSET MEDIAN IMPLANT H14MM 30X39MM

    FDA Adverse Event
    Malfunction ·LDR MÉDICAL·Product code MAX·May 13, 2023