BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    IV FLUID TRANSFER PIN

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Lewicky Chamber Maintainer

    FDA UDI
    Medetz Surgical Instruments LLC·G223159254010·Lewicky Chamber Maintainer Custom 25ga Threaded...

    Phantom

    FDA UDI
    Innovative Med·00851314007014·Surgical Aspirator: 1/3 hp. 0-3.6 scfm / 0-27....

    IMMUNOWELL CARDIOLIPIN ANTIBODY (IGM) TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    ASEPTIMINI UNIT, ADU-10

    FDA 510(k)
    FDA Class 1 ·Dental

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·October 10, 2007

    INTERGRATED APD SET

    FDA Adverse Event
    Malfunction ·VANTIVE US HEALTHCARE LLC·Product code FKX·April 4, 2025

    SECURA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·December 14, 2010

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 22, 2013

    INTEGRITY ADX DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·January 15, 2014

    UroLift System REF Catalog Number: UL400-4 Tray Contents: UroLift System with Handle Release Tool STERILE R CE 0050 Manufactured By: neotract

    FDA Recall
    Terminated ·Neotract Inc·Product code PEW·July 6, 2018