BEUDAMED
    6 results · 35ms · Sources: EU EUDAMED, US FDA

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    ANGIOMAT ILLUMENA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DISCYPHOR CATHETER SYSTEM, MODEL D01A; DISCYPHOR INTRODUCER NEEDLE, MODEL D01B

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    vascuCAP

    FDA 510(k)
    FDA Class 2 ·Radiology

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 23, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·February 15, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·January 18, 2011