BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    APRO 55 Catheter and Alembic Aspiration Tubing

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MONACO

    FDA 510(k)
    FDA Class 2 ·Radiology

    TIDAL WAVE SP MODEL 710/715 AND 715

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 21, 2025

    MAXIMUM HEMOSTASIS INTRODUCER 6F, 12CM ACT SHEATH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code DYB·March 28, 2007

    EVIS EXERA II XENON LIGHT SOURCE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GCT·July 22, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·November 6, 2014

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 18, 2013