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

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    LUMENON XENON LIGHT SOURCE

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

    Prefix Fixator

    FDA UDI
    ORTHOFIX SRL·18033509851773·TRANSFIXING PIN, THREAD L 50 MM STERILE SHAFT D...

    Vu aPod™ - L

    FDA UDI
    Seaspine Orthopedics Corporation·10889981118075·Wide Standard Implant Caddy, 50mm

    Astraguard

    FDA UDI
    S D I DIAGNOSTICS INC·B279S297992050·bacterial viral filter

    ETEST Eravacycline (ERV) (0.002 – 32 µg/mL)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    IMMUNOCAP ALLERGEN D201, HOUSE DUST MITE, MODEL 4-4896-01

    FDA 510(k)
    FDA Class 2 ·Immunology

    RADIFOCUS OPTITORQUE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·March 7, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    ATTAIN STARFIX

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·August 8, 2014

    OPTITORQUE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·Product code DQO·January 20, 2021