BEUDAMED
    22 results · 24ms · Sources: EU EUDAMED, US FDA

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    Biomet Bone Cement R

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPTIPAC 60 REFOB BONE CMT R-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·May 11, 2026

    BIOMET BONE CMENT R 1X40 JP

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·May 22, 2025

    REFOBACIN BONE CEMENT R 1X40-3

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·June 18, 2025

    OPTIPAC 80 BIOMET BC R

    FDA Adverse Event
    Death ·BIOMET FRANCE S.A.R.L.·Product code LOD·April 9, 2026

    BIOMET BONE CEMENT R 40 -3

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·July 31, 2025

    BIOMET BONE CMENT R 1X40 JP

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·June 17, 2025

    OPTIPAC 60 REFOB BONE CMT R-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·February 5, 2025

    OPTIPAC 60 REFOB BONE CMT R-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·February 5, 2025

    BIOMET BONE CMENT R 1X40 JP

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·October 8, 2025

    BIOMET BONE CMENT R 1X40 JP

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·October 8, 2025

    BIOMET BONE CMENT R 1X40 JP

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·April 8, 2025

    OPTIPAC 80 BIOMET BC R

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·February 21, 2025

    DIGITAL DIAGNOSTIC X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    EMU-GRAPH EMULATOR, MODEL CI 131

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 3, 2025

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·June 17, 2011

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code NVY·January 13, 2014

    MX-PRO R-3 AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·June 17, 2013

    PEN NDL 32G 4MM PRO 100 BOX 1200 CA

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·May 29, 2024