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

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    ADVANCE PRESSURE MONITOR LINE, HIGH PRES., ADMINI.

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756734134·CUSTOM BASIN PACK

    OMNIFIT CONSTRAINED ACETABULAR BEARING INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DYNATEX PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    STAPLE, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 26, 2014

    COLLEAGUE CXE VOLUMETRICINFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 12, 2010

    DIGITAL RADIOGRAPHY CXDI-70C WIRELESS

    FDA Adverse Event
    Malfunction ·CANON, INC·Product code MQB·December 31, 2012

    TI LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code NKG·November 20, 2017

    TI LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code NKG·June 9, 2017