BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    esolution® Esophageal Retractor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THERAPY ABLATION CATHETER

    FDA Adverse Event
    Malfunction ·IRVINE BIOMEDICAL, A ST. JUDE MEDICAL COMPANY·Product code OAD·June 25, 2010

    Mitsar-EEG

    FDA 510(k)
    FDA Class 2 ·Neurology

    GOTFRIED PHYSIOLOGICAL HIP (PH) NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 2, 2025

    COAGUCHEK XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·November 7, 2008

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·September 1, 2011

    23 GAUGE HIGH SPEED VITRECTOMY CUTTER

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB .·Product code HQC·July 19, 2013

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 18, 2018