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

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    Filters Status: Injury ×

    56MM AND R3 ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBL·September 14, 2018

    INTERSTIM LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·May 7, 2008

    VERIFLEX¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·January 10, 2013

    SINGLE USE ELECTROSURGICAL HEMOSTATIC FORCEPS

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·November 13, 2023

    SINGLE USE ELECTROSURGICAL KNIFE KD-612

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·November 13, 2023

    EVIS LUCERA SMALL INTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDA·November 13, 2023

    SINGLE USE ELECTROSURGICAL KNIFE

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·November 13, 2023

    SYSTEM, APPENDAGE CLOSURE, LEFT ATRIAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·September 3, 2025