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

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    Filters FDA Adverse Event × Regulation: Us FDA × Clear all

    PERSONA® TRABECULAR METAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·January 7, 2026

    G7 STR MONOBLOCK SHELL INSRTR

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LXH·August 21, 2019

    DEVILBISS TRAVELER

    FDA Adverse Event
    Malfunction ·DEVILBISS HEALTHCARE·Product code EPN·January 26, 2018

    PERSONA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·November 24, 2025

    OFFSET FLEX CLAMP BROACH HANDLE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LXH·November 25, 2019

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·May 16, 2019

    OFFSET FLEX CLAMP BROACH HNDL E

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LXH·November 25, 2019

    PRIMA HUMERAL SYSTEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code PHX·May 4, 2026

    EPI CLENZ HAND SANITIZER

    FDA Adverse Event
    Other ·EPI CLENZ·Product code KOY·October 7, 2003

    CAUD-A KATH CATHETER

    FDA Adverse Event
    Malfunction ·EPI-MED·Product code GCB·March 15, 1995

    EPI-MED

    FDA Adverse Event
    Malfunction ·EPI-MED·Product code BSO·June 24, 2003

    ALPHA-STIM TECHNOLOGY

    FDA Adverse Event
    Injury ·EPI, INC·Product code JXK·December 19, 2013

    PN RELION 32G X 4MM 3B TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FMI·June 11, 2021

    PN RELION 31G X 8MM 3B TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FMI·June 11, 2021

    PN RELION 31G X 6MM 3B TW 50CT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FMI·May 14, 2021

    EBI ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·EBI·Product code KWQ·April 14, 2008

    BACT/ALERT BPN

    FDA Adverse Event
    Malfunction ·BIOMÉRIEUX, INC·Product code MZC·September 9, 2022

    BACT/ALERT BPN

    FDA Adverse Event
    Malfunction ·BIOMÉRIEUX, INC·Product code MZC·September 24, 2022

    EP MED SYSTEM

    FDA Adverse Event
    Injury ·EP MED SYSTEM·Product code DTA·September 8, 2003

    FILTERWIRE EX SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC/EPI·Product code MUN·November 21, 2001