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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    MAGNATEK 40

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IC-PRO SYSTEM, VERSION 3.1.0.4

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPY Elite Intraoperative Perfusion Assessment System

    FDA 510(k)
    FDA Class 2 ·Radiology

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 31, 2013

    COLLEAGUE 3 TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP CE FRENC

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 9, 2011

    OPTIFLUX 160NRE DIALYZER FINISHED ASSY.

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FJI·June 25, 2014