BEUDAMED
    14 results · 21ms · Sources: EU EUDAMED, US FDA

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    LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·August 28, 2020

    LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code FAQ·August 14, 2024

    LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·December 13, 2020

    LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·March 4, 2020

    LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·May 14, 2018

    LEG BAG WITH FLIP-FLO VALVE AND LATEX STRAPS, 32 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·April 25, 2019

    LEG BAG WITH FLIP-FLO VALVE AND LATEX STRAPS

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·April 29, 2019

    V-PRO 1 PLUS STERILIZER

    FDA Adverse Event
    STERIS MEXICO, S. DE R.L. DE C.V.·Product code MLR·May 15, 2014

    CARELINK PROGRAM W/TELEMETRY C

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·October 31, 2012

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·August 18, 2010

    1018233-2018-05488

    FDA Adverse Event
    Malfunction ·November 16, 2018

    LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·September 14, 2022

    URIPLAN LEG BAG DRUG TARIFF

    FDA Adverse Event
    Malfunction ·PRODUCTOS PARA EL CUIDADO DE LA SALUD -9611590·Product code KNX·May 12, 2016

    LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·August 30, 2019