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

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    Filters Status: Malfunction ×

    VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·June 8, 2023

    VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·June 8, 2023

    VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·June 8, 2023

    VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·June 8, 2023

    VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·June 8, 2023

    VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·June 8, 2023

    ARCHITECT TOTAL B-HCG

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code DHA·April 27, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·April 27, 2020