BEUDAMED
    10 results · 20ms · 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.
    Filters Regulation: Us FDA ×

    CarboClear® Posterior Cervical Screw System; CarboClear® Hybrid Posterior Cervical Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Armada

    FDA UDI
    Nuvasive, Inc.·00887517223043·ARM15T Screw, 4x45mm PLS

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017989·K-Wire, Single Ended, Trocar Point, Diameter Si...

    NA

    FDA UDI
    Exactech, Inc.·10885862525468·TRIAL, TIBIAL ADAPTOR, PLATE, SIZE 4.5

    uWS-Angio Pro

    FDA 510(k)
    FDA Class 2 ·Radiology

    FreedomEdge Syringe Infusion System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD CONNECTOR LUER LOCK C45

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·May 17, 2019

    VENTAK PRIZM HE DR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008

    HYDROLINE PULSEWAVE SYSTEM

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, INC.·Product code GBX·June 25, 2013

    LIFESTENT VASCULAR STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code FGE·August 10, 2011