BEUDAMED
    1,852 results · 26ms · Sources: EU EUDAMED, US FDA

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    NEOMED*

    FDA UDI
    Avanos Medical, Inc.·00350770002026·Oral Syringe F-F Coupler NonSterile

    NeoMed Syringe-to-Syringe Coupler

    FDA UDI
    NEOMED, INC.·10817584010557·NeoMed Oral Syringe Coupler, Female/Female, For...

    Disposable Biopsy Valve

    FDA UDI
    Yangzhou Fartley Medical Instrument Technology Co., Ltd·06936603217139·

    MIDAS REX MR8

    FDA Adverse Event
    Malfunction ·MDT POWERED SURGICAL SOLUTIONS·Product code HBE·March 13, 2026

    3002807968-2017-00048

    FDA Adverse Event
    Malfunction ·December 22, 2017

    3002807968-2017-00049

    FDA Adverse Event
    Malfunction ·December 22, 2017

    3002807968-2018-00058

    FDA Adverse Event
    Malfunction ·October 11, 2018

    3002807968-2018-00059

    FDA Adverse Event
    Malfunction ·October 11, 2018

    UNKNOWN OXFORD BEARING

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 4, 2023

    Disposable Biopsy Valve

    FDA UDI
    Yangzhou Fartley Medical Instrument Technology Co., Ltd·06936603225615·

    3002807968-2018-00004

    FDA Adverse Event
    Malfunction ·January 10, 2018

    PICO70

    FDA Adverse Event
    Malfunction ·RADIOMETER MEDICAL APS·Product code JKA·October 19, 2020

    UNKNOWN OXFORD BEARING

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 4, 2023

    UNKNOWN REFOBACIN BONE CEMENT R

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·December 11, 2023

    UNKNOWN OXFORD FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 4, 2023

    UNKNOWN OXFORD TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 4, 2023

    DREAMSTATION AUTO BIPAP

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 29, 2023

    UNKNOWN REFOBACIN BONE CEMENT R

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·December 11, 2023

    TITANIUM IMPLANTABLE PORT

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS·Product code LJT·October 9, 2018

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·June 8, 2020