BEUDAMED
    5 results · 24ms · 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 ×

    LTV 1200 VENTILATOR

    FDA Adverse Event
    Malfunction ·VYAIRE MEDICAL, INC·Product code CBK·January 17, 2024

    SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·June 8, 2015

    SYSTEM 90T

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·November 9, 1999

    FIXED ABUTMENT: PREANGLED, 15 DEGREE, 2MM, OMNILOC, 4.0

    FDA Adverse Event
    Injury ·SULZER CALCITEK·Product code DZE·February 24, 1998

    MEDIUM A/P LIPPED TIBIAL INSER

    FDA Adverse Event
    Malfunction ·HOWMEDICA OSTEONICS·Product code HSH·August 30, 2001