BEUDAMED
    4 results · 16ms · 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 Status: Injury ×

    FEM. MODULAR HEAD - M Ø28MM 2

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LPH·October 21, 2022

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·January 10, 2019

    S-ROM*SLEEVE PRX ZTT, 16B-LRG

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ¿ REG. # 1219655·Product code LPH·July 1, 2013

    CORTICAL BONE SCREW D.4,5 L.20MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code PHX·April 24, 2024