BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    Instrument Case

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Plasdent Disposable Barrier Sleeves and Barrier Film

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

    GLYCOMARK

    FDA 510(k)
    FDA Class 2 ·Hematology

    COCHLEAR OSIA OSI300 IMPLANT

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

    COCHLEAR OSIA OSI300 IMPLANT

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code PFO·January 15, 2024

    COCHLEAR OSIA OSI300 IMPLANT

    FDA Adverse Event
    Injury ·COCHLEAR LIMITED·Product code PFO·January 15, 2024

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·November 13, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 1, 2011

    UNKNOWN ASR CUP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ? REG. # 8010379·Product code KWA·July 17, 2013