BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    DYNAMOMETER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    866.5750 RADIOALLERGOSORBENT IMMUNLOGICAL TEST SYS

    FDA 510(k)
    FDA Class 2 ·Immunology

    THORATEC CENTRIMAG PRIMARY CONSOLE

    FDA Adverse Event
    Malfunction ·THORATEC SWITZERLAND GMBH·Product code DWA·June 25, 2014

    ENTRUST VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011

    InterGard Knitted Collagen Coated Vascular prostheses marketed under 510(k) # K964625; InterGard Woven Collagen Coated Vascular prostheses marketed under 510(k} #K970843 and K984294.

    FDA Recall
    Terminated ·Intervascular S.A.S. Zone Industrielle Athelia I La Ciotat Cedex France·Product code DSY·December 9, 2009