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

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    MEDI-DX 7000

    FDA 510(k)
    FDA Class 1 ·Neurology

    HEARING CHECKER(TM), DESKTOP MODEL

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CYTOQUANT A-549 CELLS, CATALOG #02-201

    FDA 510(k)
    FDA Class 1 ·Hematology

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·May 30, 2014

    CAPSURE SP

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·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