BEUDAMED
    1,622 results · 24ms · Sources: EU EUDAMED, US FDA

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    ARROW CVC SET: 2-LUMEN 4 FR X 8 CM

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL INC.·Product code DQY·May 15, 2018

    INFUSOMAT SPACE

    FDA Adverse Event
    Malfunction ·B.BRAUN MELSUNGEN AG·Product code FRN·June 22, 2023

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR-CALIF·Product code NJE·June 6, 2014

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR-CALIF·Product code NJE·June 6, 2014

    UNKNOWN EVD CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·October 21, 2016

    CHLORAPREP UNKNOWN

    FDA Adverse Event
    Injury ·CAREFUSION 213, LLC 0113·Product code KXG·October 25, 2021

    REMUNITY SUBCUTANEOUS DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·DEKA RESEARCH & DEVELOPMENT CORP.·Product code QJY·September 10, 2024

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·November 13, 2012

    BIOPATCH, UNKNOWN SIZE/PRODUCT ID

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code FRO·September 12, 2023

    NIM® EMG - ENDOTRACHEAL TUBE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code ETN·September 27, 2023

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·September 9, 2025

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 1, 2026

    CHLORAPREP UNKNOWN

    FDA Adverse Event
    Injury ·CAREFUSION 213, LLC 0113·Product code KXG·January 21, 2022

    EXPORT AP ASPIRATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC, INC·Product code DXE·October 4, 2019

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code NJE·March 16, 2016

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·March 16, 2016

    NORDIPEN 5

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S·Product code FMF·July 28, 2016

    PIPELINE FLEX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·July 5, 2019

    CADD MEDICATION CASSETTE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·January 10, 2025

    UNSPECIFIED CADD MEDICATION CASSETTE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·January 9, 2025