BEUDAMED
    32 results · 61ms · Sources: EU EUDAMED, US FDA

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    SPINA

    FDA Adverse Event
    Malfunction ·NORTH AMERICAN MEDICAL CORP·Product code ITH·August 20, 2002

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code KMW·May 9, 2014

    COTTON-LEUNG BILIARY STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·April 7, 2026

    AMPLATZER PFO OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORP.·Product code MLV·September 20, 2007

    MEDTRONIC -PREVIOUSLY, PHYSIO-CONTROL -

    FDA Adverse Event
    Injury ·MEDTRONIC EMERGENCY RESPONSE SYSTEMS·Product code MKJ·September 26, 2006

    OLYMPUS ELECTROSURGICAL UNIT

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code KNS·September 2, 2010

    DIGITAL THERMOMETER

    FDA Adverse Event
    Malfunction ·AMERICAN SCREENING CORPORATION·Product code PXH·March 10, 2021

    CORMATRIX ECM

    FDA Adverse Event
    Injury ·CORMATRIX CARDIOVASCULAR, INC.·Product code DXZ·June 20, 2013

    TENSION FREE VAGINAL TAPE - OBTURATOR UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·September 10, 2021

    EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Death ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code ODG·January 17, 2022

    HARMONIC ACE 5MM SHEAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 4, 2021

    COLOPLAST TITAN OTR. A/S - AMS 700 MS SERIES PENILE PROSTHESIS

    FDA Adverse Event
    Other ·COLOPLAST CORP., / AMERICAN MEDICAL SYSTEMS INC.·Product code FAE·August 4, 2016

    PHILLIPS

    FDA Adverse Event
    Injury ·PHILLIPS MEDICAL SYSTEMS - PHILLIPS NORTH AMERICAN CORP.·Product code DRT·March 17, 2016

    BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count sample contained in Patient Counseling Sample Toolbox -Catalog 6484755/Lot Number: 3750144)-Sterile, single use devices designed for the parenteral administration of a drug from a cartridge contained in a drug pen injector Model/Catalog Number: 320551

    FDA Recall
    Open, Classified ·Embecta Corp.·Product code FMI·June 18, 2024

    MICROVASIVE GASTROSTOMY TUBE 20FR

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL TECHNOLGIES BOSTON SCIENTIFIC CORP. EENDOSCOPY DIV.·Product code KNT·July 16, 1996

    LASER SCOPE KTP/532 12 AMP

    FDA Adverse Event
    Injury ·LASER SCOPE / AMERICAN MEDICAL SYSTEMS INNOVATION CENTER / BOSTON SCIENTIFIC CORP.·Product code GEX·July 11, 2019

    SANGUESA SA

    Importer
    🇪🇸 Spain·10 Manufacturers

    mdi Europa GmbH

    Authorized representative
    🇩🇪 Germany·132 Manufacturers·4741 Devices

    Medical Technology Promedt Consulting GmbH

    Authorized representative
    🇩🇪 Germany·194 Manufacturers·10009 Devices

    MedNet EC-REP GmbH

    Authorized representative
    🇩🇪 Germany·464 Manufacturers·5263 Devices