BEUDAMED
    35 results · 68ms · Sources: EU EUDAMED, US FDA

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    ECMO DOUBLE LUMEN VV CANNULA 28 F

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL INC.·Product code DWF·December 30, 2016

    ORIGEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC.·Product code DQO·March 13, 2002

    REINFORCED DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC.·Product code DWF·November 1, 2017

    DOUBLE LUMEN 12 FR. CANNULA

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL INC.·Product code DWF·November 17, 2003

    ORIGEN EVOLVE 3000 ML CRYOPRESERVATION BAG

    FDA Adverse Event
    Injury ·ORIGEN BIOMEDICAL, INC.·Product code KSR·October 16, 2020

    SPIKE ADAPTER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC.·Product code KJG·August 8, 2025

    CRYOSTORE CS500N

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC·Product code KSR·September 30, 2021

    ORIGEN REINFORCED DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC·Product code DWF·April 2, 2019

    ORIGEN REINFORCED DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC·Product code DWF·April 2, 2019

    ORIGEN REINFORCED DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC·Product code DWF·April 2, 2019

    ORIGEN REINFORCED DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC·Product code DWF·April 2, 2019

    ORIGEN DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC·Product code DWF·April 2, 2019

    ORIGEN REINFORCED DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC·Product code DWF·April 2, 2019

    ECMO DOUBLE LUMEN VV CANNULA

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC.·Product code DWF·February 10, 2017

    ORIGEN REINFORCED DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC·Product code DWF·April 2, 2019

    ORIGEN REINFORCED DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC·Product code DWF·April 2, 2019

    CRYOSTORE

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC.·Product code KSR·February 14, 2024

    CS550S CRYOSTORE FREEZINGBAG

    FDA Adverse Event
    Injury ·ORIGEN BIOMEDICAL, INC.·Product code KSR·October 8, 2024

    ORIGEN DUAL LUMEN CANNULA, 12 FR

    FDA Adverse Event
    Injury ·ORIGEN BIOMEDICAL, INC.·Product code DWF·October 25, 2001

    PTCA

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC.·Product code DQO·May 23, 2011