BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNK LATARJET SCREW

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code HWC·June 14, 2017

    UNK LATARJET SCREW

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code HWC·June 14, 2017

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 27, 2014

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 26, 2013

    HS III PROXIMAL SEAL SYSTEM 4.3MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·August 4, 2011

    ESSURE

    FDA Adverse Event
    Injury ·BAYER HEALTHCARE LLC·Product code HHS·August 25, 2016

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code ODP·April 1, 2019

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code ODP·April 1, 2019

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code ODP·April 1, 2019