BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    VERRES NEEDLE

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

    SSA-770A - VERSION 4, APLIO DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    ReVive PV (Peripheral Vasculature) Thrombectomy Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·January 22, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·December 17, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 14, 2014