BEUDAMED
    29 results · 83ms · Sources: EU EUDAMED, US FDA

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    BOLLE SAFETY INC

    FDA registration
    BOLLE SAFETY INC·1 product·🇺🇸 United States

    ERBE ESU MODEL VIO 300 D

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·July 6, 2023

    ERBE ICC 200 E

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·September 1, 2021

    NEWLIFE INTENSITY

    FDA Adverse Event
    Injury ·CAIRE INC.·Product code CAW·May 1, 2023

    ERBE VIO 3

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·October 21, 2024

    FREESTYLE COMFORT

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code CAW·July 3, 2023

    PRECISION MEDICAL

    FDA Adverse Event
    Injury ·PRECISION MEDICAL·Product code CAN·August 22, 2003

    LEEP SYSTEM

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HGI·June 20, 2016

    LIBERATOR

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·October 17, 2023

    COULTER® HMX HEMATOLOGY ANALYER WITH AUTOLOADER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·October 20, 2011

    COULTER® HMX HEMATOLOGY ANALYER WITH AUTOLOADER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·October 20, 2011

    ERBECRYO 2

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEH·August 12, 2020

    ERBE VIO 3

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·February 9, 2023

    INFUSOMAT SPACE

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·September 8, 2015

    ERBE VIO 300 D

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·September 1, 2017

    ERBE VIO 300 D

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·August 31, 2017

    ENDO POUCH WITH MEMORY WIRE 5X7"

    FDA Adverse Event
    Malfunction ·UNIMAX MEDICAL SYSTEMS INC·Product code GCJ·May 17, 2021

    ERBE VIO 300 S

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·July 13, 2016

    ERBE VIO 300 D

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·September 7, 2017

    LEEP PRECISION GENERATOR

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HGI·July 22, 2022