BEUDAMED
    4 results · 15ms · 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 ×

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·February 8, 2018

    NEXGEN CR-FLEX FEMORAL COMPONENT POROUS

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·January 11, 2011

    OXF ANAT BRG LT SM SIZE 7 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·January 31, 2023

    OXF TWIN-PEG CMNTD FEM SM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·January 31, 2023