BEUDAMED
    14 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ANGIOSEAL DEVICE

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL, CARDIOLOGY DIVISION·Product code MGB·March 14, 2008

    PROGREAT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 7, 2026

    PROGREAT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 7, 2026

    PROGREAT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 26, 2026

    PROGREAT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 30, 2025

    T-PIECE NEONATAL PATIENT CIRCUIT KIT, DISPOSABLE, WITH SIZE

    FDA Adverse Event
    Injury ·MERCURY MEDICAL·Product code CAI·September 29, 2015

    PROGREAT

    FDA Adverse Event
    Injury ·Product code DQO·April 30, 2021

    NEONATAL PATIENT CIRCUIT KIT

    FDA Adverse Event
    Injury ·MERCURY MEDICAL·Product code CAI·September 21, 2015

    TERUMO PROGREAT CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 25, 2022

    PROGREAT CATHETER

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DQO·March 23, 2023

    PROGREAT CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·June 20, 2023

    TERUMO PROGREAT CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·October 28, 2022

    PROGREAT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·January 10, 2025

    PROGREAT CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·October 2, 2019