BEUDAMED
    13 results · 22ms · Sources: EU EUDAMED, US FDA

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    FORZA® XP Expandable Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ANT ANGIOGRAPHIC SYRINGES, MODEL(S) 100101,102,103,100201,202,203,204,100301,200101,201,202, 203,200301,101,102,202,301

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TWIN PEAKS LUMBAR CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 5, 2025

    RELION INSULIN SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 9, 2022

    UNKNOWN BEARING COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HRY·January 17, 2018

    UNKNOWN FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDG·January 16, 2018

    UNKNOWN TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HRY·January 16, 2018

    UNKNOWN TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HRY·January 16, 2018

    UNKNOWN TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HRY·January 17, 2018

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 22, 2011

    PULSE GEN MODEL 104

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·June 17, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 15, 2014