BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    FIBEROPTIC ILLUMINATED INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    AMS GRAM-NEGATIVE IDENT. CARD

    FDA 510(k)
    FDA Class 1 ·Microbiology

    NEUROSEARCH-24 OR NRS-24

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACRYSOF IQ SINGLEPIECE IOL WITH ULTRASERT DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LLC - HUNTINGTON·Product code HQL·February 18, 2022

    SHILEY

    FDA Adverse Event
    Injury ·COVIDIEN·Product code JOH·June 27, 2014

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·January 7, 2013

    COOL PATH 7F IRRIGATED ABLATION CATHETER

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL, IRVINE·Product code OAD·November 24, 2010