BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    SOFLENS DAILY DISPOSABLE TORIC (HILAFILCON B) VISIBILITY TINTED CONTACT LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5820807550·RONGEUR

    NA

    FDA UDI
    STRYKER CORPORATION·07613327056556·Insert, Fenestrated Grasper

    RHIGENE MESACUP2 TEST- SM

    FDA 510(k)
    FDA Class 2 ·Immunology

    BAYER DIAGNOSTICS ADVIA CENTAUR TOXOPLASMA IGM ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    VERSAFITCUP CC TRIO ACETABULAR SHELL

    FDA Adverse Event
    MEDACTA INTERNATIONAL SA·Product code LZO·April 19, 2013

    CONSERVE(R) TOTAL A-CLASS

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDL·May 6, 2011

    PULSE GEN MODEL

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·July 23, 2008

    ARCHITECT CYCLOSPORINE REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code MKW·August 8, 2025

    ARCHITECT CYCLOSPORINE REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code MKW·September 4, 2025

    ABBOTT TUBE EDTA PLH 13X75 2.0 PNK

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·August 3, 2022

    ABBOTT TUBE EDTA PLH 13X75 2.0 PNK

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·September 17, 2019

    ARCHITECT CYCLOSPORINE REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code MKW·September 30, 2025