BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    FLEXIBLE REAMER, GUIDE WIRE SYSTEM

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    APEX Knee System

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

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790307000·topic Bracket, - 1° Torque, 0° Angulation for t...

    BEDPAN, SINGLE PATIENT USE, TECNOL

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DDI ULTRASONIC NEBULIZER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PLATE, FIXATION, BONE

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

    CAPSURE SP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·August 6, 2010

    PALL ULTIPOR 25 BREATHING SYSTEM FILTER

    FDA Adverse Event
    Injury ·PALL NEWQUAY·Product code CAH·July 13, 2018

    PALL ULTIPOR 100 BREATHING SYSTEM FILTER

    FDA Adverse Event
    Injury ·PALL NEWQUAY·Product code CAH·April 18, 2017