BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    AccuContour

    FDA 510(k)
    FDA Class 2 ·Radiology

    Oticon

    FDA UDI
    Oticon A/S·05707131339782·SIYA 1, KIT 312 NFM 90 L C001

    BD MICROTAINER® MAP MICROTUBE FOR AUTOMATED PROCESS K2 EDTA

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·November 2, 2018

    VENTRALEX ST HERNIA PATCH

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

    10 X 10 VISION

    FDA 510(k)
    FDA Class 2 ·Radiology

    COCHLEAR OSIA OSI300 IMPLANT

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code PFO·March 8, 2026

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·July 22, 2011

    EXTRACTOR XL TRIPLE LUMEN RETRIEVAL BALLOON

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code GCA·October 1, 2008

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·June 27, 2013