BEUDAMED
    8 results · 34ms · 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.

    MEDTRONIS(R) PACING LEADS AND LEAD ADAPTORS, MODIF

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    GLUCOSE REAGENT FOR BECKMAN SYNCHRON CX & CX DELTA SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LARYNGOSCOPE BLADES/HANDLES & LAMPS

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    CUSA EXCEL 36KHZ CURVED EXTENDED MICRO

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES(IRELAND)·Product code LFL·January 28, 2019

    CUSA EXCEL 36KHZ CURVED EXTENDED STANDARDTIP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES(IRELAND)·Product code LFL·November 19, 2018

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 18, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code LFR·December 20, 2010

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 14, 2014