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

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    OMNI-FIX, NAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VARIAX

    FDA UDI
    Stryker GmbH·07613327129076·Instrument Kit

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690182542·AK3 Femoral Distal Locating Device, 7° Bushing

    MSI

    FDA UDI
    Modern Surgical Instruments LLC·00810130203734·Round handle micro cervical curette 10", fwd an...

    MSI

    FDA UDI
    Modern Surgical Instruments LLC·B419MSI9903070·

    FLEXIBLE REAMER, GUIDE WIRE SYSTEM

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    DDI ULTRASONIC NEBULIZER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 5, 2013

    SIGMA 300 SR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·February 15, 2011

    SPRINT QUATTRO

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·August 7, 2014

    ENCOREANYWHERE

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·February 17, 2016