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

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    LEEP SYSTEM 1000 ESU GEN

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HGI·August 18, 2021

    HEMASHIELD GOLD WOVEN D.V. AORTIC ARCH VASC.

    FDA Adverse Event
    Malfunction ·MAQUET CADIOVASCULAR, LLC·Product code DSY·March 8, 2013

    COATED VICRYL PLUS (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAM·February 3, 2011

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 20, 2008

    88-000006 ROCKER W/COATED BLADE N/S

    FDA Adverse Event
    Malfunction ·DEROYAL·Product code GEI·December 8, 2000

    ADVANTAV12,COVERED STENTSYS, 6X59X120

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·June 28, 2018