BEUDAMED
    4 results · 20ms · 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 ×

    EVOLUT FX PLUS VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·November 25, 2025

    STELLARIS 25G VIT CUTTER 6/BX

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB, INC.·Product code HQC·April 3, 2013

    LIBERTY DRAIN LINE, LUER TAPER CONNECTOR

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE, REYNOSA MANUFACTURING·Product code KDJ·August 15, 2014

    S-ROM HEAD FEMRL ZIRCONIA 28+0

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code LZO·May 8, 2008