BEUDAMED
    6,270 results · 29ms · Sources: EU EUDAMED, US FDA

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    EGIS Biliary Single Bare Stent

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

    AEGIS NAVIGATION ANDA EGIS PELVIC APPLICATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    EGIS Biliary Double Bare Stent (BDB080405)

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

    EVOLUTION® ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code ESW·May 2, 2023

    HARNESS, A-E GI ADAPTER

    FDA Adverse Event
    Other ·MEDIVATORS REPROCESSING SYSTEM/DIVISION OF MINNTECH·Product code FEB·May 1, 2007

    EGI 60 ARTICULATING MED/THICK SULU

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SUR·Product code GAG·May 22, 2014

    EGI 30 CURVED TIP ARTICULATING VAS SULU

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·March 25, 2014

    GENDEX GXP DENTAL X-RAY PROCESSOR

    FDA Adverse Event
    Malfunction ·GENDEX DENTAL SYSTEMS·Product code EGY·May 27, 2010

    DENOPTIX QST DIGITAL IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·ALARA, INC.·Product code EGY·April 5, 2012

    DENOPTIX DIGITAL IMAGING SYSTEM

    FDA Adverse Event
    Injury ·DENTSPLY GENDEX·Product code EGY·November 12, 2003

    DENT X

    FDA Adverse Event
    Injury ·MOHAWK DENTAL SUPPLY CO., INC.·Product code EGY·March 16, 2007

    MAMORAY COMPACT EOS

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE GMBH·Product code EGY·December 21, 2007

    PERI-PRO

    FDA Adverse Event
    Malfunction ·AIR TECHNIQUES, INC.·Product code EGY·February 26, 2009

    PHASIX MESH

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code OOD·July 21, 2025

    ENDO GIA

    FDA Adverse Event
    Injury ·US SURGICAL PUERTO RICO·Product code GDW·August 26, 2024

    TALENT AAA

    FDA Adverse Event
    Death ·MEDTRONIC CARDIOVASCULAR·Product code MIH·July 2, 2014

    MEDTRONIC TRANSCATHETER DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·December 20, 2021

    ZILVER 635 BILIARY SELF EXPANDING METAL STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·August 18, 2022

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK MEDICAL IRELAND·Product code FGE·June 29, 2023

    ENDO GIA ULTRA

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·December 27, 2024