BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    VALVE, H-H CRUCIFORM SLIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517360410·CoRoent SI Guide, 10mm DTS

    SurgyCut

    FDA UDI
    U.S. SURGITECH INC.·00810014631769·SurgyCut Spatula with Handle Electrode, 5mm/35cm

    SurgyCut

    FDA UDI
    U.S. SURGITECH INC.·00810014632780·SurgyCut Spatula with Handle Electrode, 5mm/45cm

    Bendit2.7 Steerable Microcatheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FOTONA XP ND: YAG LASER SYSTEM FAMILY, FOTONA XP, XP-2 FOCUS, FOTONA XP CHANGER,MODEL MOO1-14F, MOO1-14F, MOO1-14F/2,

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

    INTERVERTEBAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MAX·May 5, 2014

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 15, 2012

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORP.·Product code LZG·August 2, 2010