BEUDAMED
    22 results · 25ms · Sources: EU EUDAMED, US FDA

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    Single Use Electrosurgical Knife KD-625 , Single Use Electrosurgical Knife KD-645

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517576071·CoRoent Ant TLIF Ti, 8x12x40mm 8°

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528127766·2.4 X 8mm Cannulated Headed Screw, T7

    DIGITAL DIAGNOSTIC X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    LEDEX, MODEL: WL-070

    FDA 510(k)
    FDA Class 2 ·Dental

    OPTIPAC 60 REFOB BONE CMT R-3

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

    ELECSYS FT3 III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·August 23, 2023

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·July 28, 2011

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 21, 2013

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON MANUFACTURING, LTD./HUNTINGTON·Product code MFK·September 12, 2008

    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

    ELECSYS FT3 III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·November 4, 2022

    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