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

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    TEST, RHEUM. ARTH., CARD (MACRO-VUE)

    FDA 510(k)
    FDA Class 2 ·Immunology

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690190875·A/P Cutting Block Assy, Open Style Size 3

    KHAN KINETIC TREATMENT DEVICE (KKT-M1)

    FDA 510(k)
    FDA Unclassified ·Unknown

    Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    JUMAO MEDICAL EQUIPMENT·Product code IOR·September 26, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·December 18, 2013

    CE INFUSOR LV 5, 12 PACK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·July 16, 2010

    PD Access Vascular Access Device. Escalon Vascular Access, Inc., 2440 South 179th Street, New Berlin, WI 53146: Model 78050 18 Gauge GA Doppler Guided Bare Needle Assembly, 2 3/4 in Length, 0.038 in guidewire, Sterile EO, PD Access Vascular Access Device. Model 78060 Extended 18 Gauge Doppler Guided Bare Needle Assembly, 3 1/2 in Length, 0.038 in Guidewire, Sterile EO, PD Access Vascular Access Device Model 75010 18 Gauge 2 3/4 in Length, 0.038 in guidewire, Sterile EO, SmartNeedle Vascular Access Devices

    FDA Recall
    Terminated ·Escalon Medical Corp·Product code DPW·May 5, 2010