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

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    CRYO CHECK FACTOR X DEFICIENT PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623171·PEEK Corp Core, Ø12x27mm

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902974359·INSTRUMENT 6971227 IMP TRIAL 7X12MM

    CLIRPATH TURBO EXCIMER LASER CATHETER (RX) -0.9MM, (RX) -1.4MM, (RX) -1.7MM, (RX) -2.0MM, MODEL 310-154, 314-159, 317-15

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    StarWalker

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

    QUATTRODE

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL NEUROMODULATION·Product code LGW·February 1, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 26, 2011

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE INC.·Product code LZG·July 8, 2014

    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