BEUDAMED
    10 results · 40ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ALINITY M HR HPV AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code MAQ·February 26, 2024

    ALINITY I HBSAG NEXT QUALITATIVE REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LOM·May 28, 2026

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·November 12, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 31, 2011

    COMPONENT MONITORING SYSTEM (FLATSCREEN)

    FDA Adverse Event
    Injury ·PHILIPS MEDICAL SYSTEMS·Product code DRT·July 10, 2013

    ALINITY I HBSAG NEXT QUALITATIVE REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LOM·May 8, 2025

    NONE

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·February 28, 2023

    ALINITY I HBSAG NEXT QUALITATIVE REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LOM·May 28, 2025

    ALINITY I HBSAG NEXT CONFIRMATORY REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LOM·May 8, 2025

    ALINITY I HBSAG NEXT QUALITATIVE REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LOM·March 20, 2025