BEUDAMED
    11 results · 29ms · 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

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 12, 2013

    RENAISSANCE 29

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·February 18, 2011

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·February 15, 2008

    INDUCTOS

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

    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

    SPECTRA OPTIA

    FDA Adverse Event
    Death ·TERUMO BCT·Product code LKN·January 7, 2026

    AMS 700 LGX

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

    CD HORIZON SPINAL SYSTEM

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