BEUDAMED
    10 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    9616240-2006-00344

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00342

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

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    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    BD VACUTAINER® LH 68 I.U. PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 30, 2023

    9616240-2006-00346

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 11, 2007

    PYXIS ANESTHESIA SYSTEM (PAS)

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code BRY·February 11, 2011