BEUDAMED
    4 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    IMPLANT, ENDOSSEOUS, ROOT-FORM

    FDA Adverse Event
    Injury ·J DENTAL CARE SRL·Product code DZE·August 28, 2025

    UNICEL DXH 800 COULTER CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 27, 2014

    COOL PATH DUO 7F, 1304-CP2-7-1.5(5)2-M-TE4BE1AB

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. (AF-IRVINE)·Product code OAD·November 7, 2012

    PENUMBRA SYSTEM REPERFUSION CATHETER 026

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·September 13, 2010