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 ×

    BARDIA FOLEY CATHETER SILICONE COATED K922431

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·November 1, 2021

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    PINNACLE 100 ACET CUP 52MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·January 22, 2013

    LTV

    FDA Adverse Event
    Death ·CAREFUSION 203, INC·Product code CBK·July 9, 2014