BEUDAMED
    25 results · 23ms · Sources: EU EUDAMED, US FDA

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    OxyLight 2.0

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Trifocus

    FDA UDI
    Diversified Products, Inc.·00037741220237·

    Operon

    FDA UDI
    Berchtold Holding GmbH·07613327412925·Berchtold Surgical Table, D 820

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112601·BARRON CORNEAL PUNCH 7.25MM

    InCompass®

    FDA UDI
    ZIMMER SPINE, INC.·00889024400450·

    NON-STERILE POWDER FREE BUBBLE-GUM SCENTED LATEX EXAMINATION GLOVE WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    P4 PHYSIO

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    GORE® VIABAHN® VBX BALLOON EXPANDABLE ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code PRL·March 3, 2022

    VALIANT NAVION

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·August 23, 2021

    ENDURANT STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·October 22, 2021

    ENDURANT STENT GRAFT

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·October 22, 2021

    ENDURANT STENT GRAFT

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·September 2, 2021

    VALIANT NAVION

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·August 23, 2021

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code NVN·January 13, 2014

    HEMOCUE GLUCOSE 201 MICROCUVETTES

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code CGA·June 28, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 5, 2011

    LUCIRA CHECK-IT COVID-19 TEST

    FDA Adverse Event
    Malfunction ·PFIZER, INC.·Product code QJR·July 31, 2023

    LUCIRA CHECK-IT COVID-19 TEST

    FDA Adverse Event
    Malfunction ·PFIZER, INC.·Product code QJR·July 31, 2023

    UNKNOWN MOTOR

    FDA Adverse Event
    Injury ·MDT POWERED SURGICAL SOLUTIONS·Product code HBB·December 6, 2021

    BD ULTRA-FINE¿ SHORT PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·April 4, 2022