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

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    Disposable Intermittent Catheter (TPU Catheter)

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

    Flex

    FDA UDI
    Diversified Products, Inc.·00842894172889·

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114056·J-SHAPED CANNULA 25GA ANGLED (PK/10)

    TAPERLOC COMPLETE RASP/PROVISIONAL

    FDA UDI
    Biomet Orthopedics, LLC·00880304632509·

    AEx Generator; PlasmaBlade T

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

    ELECSYS CORTISOL TEST SYSTEM, ADDITION OF SALIVA SAMPLE TYPE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CLINITEK STATUS+

    FDA Adverse Event
    SIEMENS HEALTHCARE DIAGNOSTICS·Product code JIL·May 16, 2016

    I-STAT EC8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE INC.·Product code CHL·March 4, 2025

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·November 7, 2008

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 31, 2011

    OPTIFLUX 200NRE DIALYZER FINISHED ASSY.

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING·Product code FJI·July 18, 2013