BEUDAMED
    5 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ITREL 3

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·July 8, 2009

    BD VACUTAINER® PST¿ GEL AND LITHIUM HEPARINN (LH) BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 2, 2018

    COULTER® LH500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·April 3, 2013

    DEPUY ASR FEM IMPLANT SZ 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KXA·March 17, 2011

    HICKMAN 9.6 FR SINGLE LUMEN CV CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC (BASD)·Product code LJS·April 25, 2008