BEUDAMED
    11 results · 39ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    AMS 700 LGX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code JCW·September 23, 2025

    AMS 700 LGX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code JCW·September 2, 2025

    AMS 700 LGX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code JCW·January 19, 2026

    M2A 38MM MOD HD -3MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 12, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·August 11, 2014

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·February 15, 2008

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 25, 2012

    INSORB 30 STAPLER

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GAG·December 29, 2020

    FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·April 2, 2020

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·November 16, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·February 22, 2021