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

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    Filters FDA Adverse Event ×

    INFUSION DEVICES - UNKNOWN

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·July 7, 2024

    INFUSION DEVICES - UNKNOWN

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·July 7, 2024

    INFUSION DEVICES - UNKNOWN

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·July 7, 2024

    INFUSION DEVICES - UNKNOWN

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·July 7, 2024

    INFUSION DEVICES - UNKNOWN

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·July 7, 2024

    SYMBIQ SINGLE CHANNEL

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 29, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013

    NI

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code KWQ·November 19, 2010

    BALL HEADS: MECTACER BIOLOX OPTION Ø 32

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·February 21, 2020