BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    4F NYLEX ANGIOGRAPHIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURGISTAR

    FDA UDI
    SURGISTAR, INC.·00878799003737·

    SURGISTAR

    FDA UDI
    SURGISTAR, INC.·00878799006066·

    KeraStat(R) Gel

    FDA 510(k)
    FDA Unclassified ·Unknown

    PARAMOUNT VBR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 13, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·February 14, 2013

    SPECTRANETICS LASER SHEATH II

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·January 13, 2011