BEUDAMED
    2,849 results · 33ms · Sources: EU EUDAMED, US FDA

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    Koala

    FDA UDI
    INSPIRATION HEALTHCARE GROUP PLC·05060195341208·Koala Warming System KOR-FLN

    ARCHITECT C4000 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 19, 2016

    WATCHMAN FLX LEFT ATRIAL APPENDAGE CLOSURE DEVICE WITH DELIVERY SYSTEM

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·May 15, 2025

    WATCHMAN FLX LEFT ATRIAL APPENDAGE CLOSURE DEVICE WITH DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·May 15, 2025

    PRO 6000 W/LARGE CRADLE

    FDA Adverse Event
    Malfunction ·WELCH ALLYN INC.·Product code FLN·June 10, 2022

    OOK SNOW ALL

    FDA Adverse Event
    Injury ·UMANO MEDICAL INC·Product code FLN·December 10, 2025

    OOK SNOW

    FDA Adverse Event
    Malfunction ·UMANO MEDICAL INC·Product code FLN·December 9, 2025

    OOK SNOW

    FDA Adverse Event
    Injury ·UMANO MEDICAL INC·Product code FLN·December 10, 2018

    ARGON PATIENT MONITORING SET

    FDA Adverse Event
    Malfunction ·MAXXIM MEDICAL, INC.·Product code FLN·August 22, 1997

    FLOW DETECTOR

    FDA Adverse Event
    Injury ·ABBOTT LABORATORIES·Product code FLN·July 11, 1997

    ARGON PATIENT MONITORING KIT

    FDA Adverse Event
    Malfunction ·MAXXIM MEDICAL ARGON DIV.·Product code FLN·April 18, 1997

    ARGON PATIENT MONITORING SET

    FDA Adverse Event
    Injury ·*·Product code FLN·May 2, 1997

    ARGON

    FDA Adverse Event
    Injury ·MAXXIM MEDICAL·Product code FLN·May 2, 1997

    LEVELERT II FLUID LEVEL SENSOR

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code FLN·January 17, 2017

    ARGON PATIENT MONITORING KIT

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL·Product code FLN·March 25, 1997

    ARGON PVC EXTENSION TUBE & STOPCOCK

    FDA Adverse Event
    Injury ·ARGON MEDICAL·Product code FLN·March 25, 1997

    ARGON PT MONITORING KIT

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL·Product code FLN·March 25, 1997

    CENTRELLA FRAME

    FDA Adverse Event
    Malfunction ·HILL-ROM BATESVILLE·Product code FLN·March 3, 2022

    Monitor, Electric For Gravity Flow Infusion Systems

    FDA classification
    FDA Class 2 ·Monitor, Electric For Gravity Flow Infusion Systems

    SHEN ZHEN SHI FAN FEN SHU TECHNOLOGY CO., LTD.

    FDA registration
    SHEN ZHEN SHI FAN FEN SHU TECHNOLOGY CO., LTD.·1 product·🇨🇳 China