BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ABBOCATH-T 20G 1-1/4IN

    FDA Adverse Event
    Malfunction ·AMSINO MED CO LTD, CONTRACT MFR FOR HOSPIRA INC.·Product code FOZ·March 3, 2011

    ABBOCATH-T 26 GA. COLOUR WHITE (500/CASE)

    FDA Adverse Event
    Injury ·AMSINO MEDICAL CO., LTD, CONTRACT MANUFACTURER FOR HOSPIRA INC.·Product code FOZ·May 24, 2012

    ABBOCATH-T 20G 2IN

    FDA Adverse Event
    Injury ·AMSINO MEDICAL CO., LTD, CONTRACT MFR FOR HOSPIRA INC.·Product code FOZ·July 21, 2011

    ABBOCATH-T 20G 2IN

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD., CONTRACT MANUFACTURER FOR HOSPIRA INC.·Product code FOZ·September 11, 2012

    ABBOCATH-T 20G 1-1/4IN

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD. (CONTRACT MFR FOR HOSPIRA, CO)·Product code FOZ·August 6, 2013

    ABBOCATH-T 26G

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD.·Product code FOZ·September 11, 2013

    ABBOCATH-T 20G 1-1/4IN

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD, CONTRACT MFR FOR HOSPIRA INC.·Product code FOZ·October 15, 2010

    ABBOCATH-T 20G 1-1/4

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD·Product code FOZ·April 27, 2009

    ABBOCATH-T 20G 1-1/4IN

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD., CONTRACT MFR FOR HOSPIRA, INC.·Product code FOZ·August 6, 2013