BEUDAMED
    556 results · 21ms · Sources: EU EUDAMED, US FDA

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    LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LANDANGER

    FDA UDI
    LANDANGER·03661219304340·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694018982·2.0mm X 11mm Cannulated Headless Screw

    External Fixation

    FDA UDI
    Life Spine, Inc.·00190837023270·165mm Threaded Rod

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613004026·Sideport Knife, Angled, 1.1mm Blade, Full Handl...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694068383·Cannulated 2.0 x 11mm Headless Screw Sterile Qty 5

    ECLIPSE TREATMENT PLANNING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    COPD LIQUID OXYGEN PORTABLE, MODEL 300P

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SANTORINI Corpectomy Cage System

    FDA UDI
    VB Spine LLC·10888857243118·Cage Inserter, Inner Shaft

    ISOLINE

    FDA Adverse Event
    Malfunction ·SORIN BIOMEDICA CRM S.R.L.·Product code MRM·January 17, 2011

    ROTOPRONE THERAPY

    FDA Adverse Event
    Malfunction ·KCI USA, INC.·Product code IKZ·May 26, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·September 13, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·May 23, 2011

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·March 18, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013

    UNICEL DXC 800 SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC·Product code JJE·July 15, 2011

    LIFEPAK 9 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·September 18, 2008

    INTEGRIS H5000C/ALLURA 9C

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code IZI·February 15, 2011

    QUICK FLEX LV LEAD

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code OJX·April 28, 2011

    PERMANENT DEFIBRILLATOR ELECTRODES

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code NVY·August 12, 2023