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

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    DIRECT PERORAL CHOLANGIOSCOPY BALLOON

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

    MegaBeam

    FDA UDI
    WISDOM MEDICAL TECHNOLOGY, LLC·00869851000382·end emitting laser fiber, single use, 600 micro...

    andorate® 2-piece Cleaning Adapter + 3-piece Valve Kit

    FDA UDI
    GA Health Company Limited·04897106958016·

    MegaBeam® Fiber Optic Delivery System with Additional Tips and Handpiece

    FDA UDI
    Ceram Optec SIA·04049089100528·

    MegaBeam

    FDA UDI
    WISDOM MEDICAL TECHNOLOGY, LLC·00859337007127·end emitting laser fiber, single use, 600 micro...

    Mariner Deformity

    FDA UDI
    Seaspine Orthopedics Corporation·10889981256258·Tri-Flat Tap, 9.5mm

    MegaBeam

    FDA UDI
    WISDOM MEDICAL TECHNOLOGY, LLC·00859337007134·end emitting laser fiber, single use, 600 micro...

    Surgical Kit

    FDA UDI
    BICON, LLC·00813110024060·Advanced Surgical Kit

    RIVA Pedicle Screw System

    FDA UDI
    XENIX MEDICAL LLC·00840493414553·Nav Awl-Tip Pedicle Tap, 9.5mm

    Zavation

    FDA UDI
    Zavation LLC·00197157009687·9.5mm TAP

    MODEL I0-3DUIMS 3D ULTRASOUND MANAGEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    OXYGEN SENSORS, MODELS CIR, C2R, R13, R15, RI7MED, R22MED, R23, R24MED, R29MED, T1, T2,T4, T7 & UFO130

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GALAXY G3 XSFT 2MM X 2CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·January 25, 2021

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·January 25, 2022

    CURRENT PLUS VR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 9, 2013

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 19, 2014

    ACCU-CHEK ® INFORM METER

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·May 24, 2011

    ONYX

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 23, 2024

    NAVISTAR¿ ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code DRF·October 25, 2022

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 23, 2024