BEUDAMED
    14 results · 29ms · Sources: EU EUDAMED, US FDA

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    Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Orange)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741926350·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674192635060·

    APOLONIA LASER IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ALCATEL-LUCENT TELEHEATH MANAGER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 22, 2025

    COPIOS PERICARDIUM MEMBRANE

    FDA Adverse Event
    Injury ·Product code NPL·June 10, 2020

    U BY KOTEX SLEEK

    FDA Adverse Event
    Malfunction ·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·August 31, 2018

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 22, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·June 27, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Death ·CPI - DEL CARIBE·Product code NVY·August 5, 2011

    U BY KOTEX SLEEK

    FDA Adverse Event
    Malfunction ·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·June 27, 2018

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F-7F

    FDA Adverse Event
    Malfunction ·CORDIS SANTA CLARA·Product code MGB·August 26, 2022

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F-7F

    FDA Adverse Event
    Malfunction ·CORDIS SANTA CLARA·Product code MGB·August 25, 2022