BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019

    CLYDESDALE PTC SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·October 17, 2019

    SIGMA CRVD XLK INS 2 10MM

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code JWH·May 29, 2013

    N/A

    FDA Adverse Event
    Injury ·EL. EN. ELECTRONIC ENGINEERING SPA·Product code GEX·September 21, 2018

    UNKNONW

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·October 9, 2018

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019

    DEKA SMARTXIDE2

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·April 6, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·July 7, 2022

    DEKA SMARTXIDE2

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·November 3, 2023