BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SALINE BREAST IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE, LLC·Product code FWM·February 12, 2020

    DEXTRUS 4137

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·February 13, 2013

    CAPSURE EPI

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·March 1, 2011

    BAXTER

    FDA Adverse Event
    Malfunction ·Product code FPA·February 22, 2008

    IMAJIN SILICONE HYDROGEL DOUBLE LOOP URETERAL STENT KIT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·August 28, 2023

    VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT KIT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·July 6, 2023