BEUDAMED
    9 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PTERYFIT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 23, 2024

    AISYS

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·January 15, 2016

    PTERYFIT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·February 25, 2025

    PTERYFIT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·July 15, 2024

    PTERYFIT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·July 14, 2024

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F/7F

    FDA Adverse Event
    Injury ·ACCESSCLOSURE, INC.·Product code MGB·March 12, 2013

    PRISM HIV O PLUS

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code MZF·February 24, 2011

    INDURA

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code LKK·February 15, 2008

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·January 13, 2022