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

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    BOWIE-DICK TEST CARD CATALOG NUMBER 008018

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Precept

    FDA UDI
    Nuvasive, Inc.·00887517387981·PRECEPT Screw Shank, 7.0x45mm Modular

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809916497353·Long-arm Multi-Axial Fenestrated Screw, Ø7.0 x ...

    Arthrex

    FDA UDI
    Provision·B504OMAR8970450·

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867133891·DRILL BIT, 4.5MM

    MODEL 6208,6209,6210,6211,6212,6214 (PLI'S)

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SC-1000 WITH SUFFIXES (SCAN CONVERTER)

    FDA 510(k)
    FDA Class 2 ·Radiology

    VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·June 26, 2014

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 11, 2010

    PINNACLE MTL INS NEUT40IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·January 4, 2013