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

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    ULTRASOUND TRANSDUCER DRAPE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CRYOSPRAY ABLATION SYSTEM, MODEL CU 8407020500

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Materialise Glenoid Positioning System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 21, 2013

    QUATTRO SECURE S

    FDA Adverse Event
    MEDTRONIC, INC.·Product code LWS·December 17, 2010

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·July 8, 2014

    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