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

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    SUTURE REMOVAL KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    J105 JAMES SURGICAL SYSTEM I/A PACK

    FDA 510(k)
    FDA Class 1 ·Neurology

    SYNTHES MAXILLOFACIAL TITANIUM MICRO SET

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 17, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 17, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 17, 2024

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES·Product code MIH·November 29, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 5, 2014

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 20, 2012

    BD BBL¿ MGIT¿ OADC ENRICHMENT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·May 13, 2024

    6X12 MILAGRO INTERFRENCE SCREW

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEI·November 2, 2018