BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LINER #L FOR MOBILE LINER Ø42

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·January 5, 2022

    EQUINOXE CAGE GLENOID SMALL, ALPHA

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·August 1, 2023

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·May 8, 2013

    TERUMO CERTRIFUGAL SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWA·May 16, 2011

    SAGB QUICK CLOSE

    FDA Adverse Event
    Malfunction ·OBTECH MEDICAL SARL·Product code LTI·August 5, 2008

    SMR HUMERAL HEAD Ø48 MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWT·May 8, 2024

    COBALT¿ XT HF QUAD CRT-D MRI SURESCAN¿

    FDA Adverse Event
    Malfunction ·MEDTRONIC EUROPE SARL·Product code NIK·August 11, 2023

    ATTAIN ABILITY MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·February 26, 2024

    SMR REVERSE FINNED HUMER. BODY

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code PHX·June 14, 2023