BEUDAMED
    1,238 results · 29ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Injury ×

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·January 3, 2012

    SUREFIT DISPERSIVE ELECTRODE

    FDA Adverse Event
    Injury ·CONMED ELECTROSURGERY·Product code GEI·November 20, 2010

    CAUTERY GROUND PAD

    FDA Adverse Event
    Injury ·CONMED CORP.·Product code GEI·May 25, 1994

    DRESSING PRIMAPORE 2"X3"

    FDA Adverse Event
    Injury ·UNK·Product code KGX·April 19, 2021

    CENTRAL LINE

    FDA Adverse Event
    Injury ·Product code FOZ·October 8, 2021

    VALLEYLAB

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·March 20, 2026

    PROPLATE

    FDA Adverse Event
    Injury ·BIOPROTECH INC.·Product code GEI·August 13, 2025

    CENTRAL LINE

    FDA Adverse Event
    Injury ·UNK·Product code FOZ·January 5, 2022

    PICC LINE

    FDA Adverse Event
    Injury ·UNK·Product code LJS·December 20, 2024

    INF SET CLEO 31" 9MM

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code FPA·October 29, 2020

    UNKNOWN_MEDICAL_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER MEDICAL-KALAMAZOO·Product code FNM·June 4, 2013

    REM PAD

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES, LP (NORTHPOINT SERVICES)·Product code GEI·March 9, 2026

    PLUME PEN ULTRA

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code GEI·March 9, 2026

    FORCE 2 GENERATOR

    FDA Adverse Event
    Injury ·VALLEYLAB·Product code GEI·June 9, 2004

    MEDLINE

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES LP·Product code GEI·April 30, 2026

    HICKMAN CATHETER

    FDA Adverse Event
    Injury ·UNK·Product code LJS·November 28, 2016

    VALLEY LAB BOVIE FORCE FX

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·September 16, 2013

    HICKMAN CATHETER

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS, INC.·Product code LJS·February 18, 2020

    TUNNELED LINE

    FDA Adverse Event
    Injury ·UNKNOWN·Product code LJS·January 8, 2025

    REM PAD

    FDA Adverse Event
    Injury ·UNK·Product code GEI·August 22, 2024