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

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    Filters Status: Injury ×

    AP LRG W/RAPIDPORT EZ

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·February 15, 2011

    VUELOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020

    VEULOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020

    VEULOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020

    VEULOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020

    BD PHOENIX¿ PMIC/ID-107

    FDA Adverse Event
    Injury ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·December 18, 2023

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·December 4, 2025