BEUDAMED
    14 results · 20ms · 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 ×

    TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517967367·Brigade Lateral, 12x34x24mm 15°

    XPS® HANDPIECE - VISAO®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·December 9, 2015

    XPS® HANDPIECE - VISAO®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·January 8, 2016

    TONOMITOR (TM) + SUMP

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    KIMBERLY-CLARK KC100 SURGICAL DRAPES, MODEL KC 100, KIMBERLY-CLARK KC100 SURGICAL EQUIPMENT COVERS, MODEL KC 100

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

    XPS HANDPIECE - VISAO

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·November 2, 2021

    DRILL 3334800 VISAO 80K HANDPIECE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ERL·July 2, 2013

    XPS® HANDPIECE - VISAO®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ERL·December 1, 2017

    XPS® HANDPIECE - VISAO®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ERL·December 1, 2017

    SINGLE ULTRASONIC DISSECTOR

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code LFL·June 27, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·February 1, 2013

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 31, 2011

    XPS® HANDPIECE - VISAO®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·June 9, 2016