BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    LIFESHIELD PRIMARY I.V. SET WITH BACKCHECK VALVE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293265·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771049514·K-Wires, Double Trocar Threaded, .062-inch (1.6...

    X-RAY DIAG. TABLE DT-KCS

    FDA 510(k)
    FDA Class 2 ·Radiology

    G3™ Active Plate® Miniature System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GORE DRYSEAL SHEATH

    FDA Adverse Event
    Death ·W. L. GORE ASSOCIATES·Product code DYB·June 22, 2012

    HIRES 90K IMPLANT

    FDA Adverse Event
    Injury ·ADVANCED BIONICS LLC·Product code MCM·June 30, 2014

    ESSURE

    FDA Adverse Event
    Injury ·BAYER·Product code HHS·August 5, 2015

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·February 21, 2013

    KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE

    FDA 510(k)
    FDA Class 2 ·Neurology