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

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    NBD HEAD SCREW

    FDA 510(k)
    FDA Class 2 ·Neurology

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496050377·TOP, SIZE S, NERO, MICRO-MASSAGING TOP WITH A T...

    MASIF POWDER-FREE PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MIMIMED SIL-SERTER INFUSION SET INSERTION SYSTEM, MODEL 385

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HEMICAP/UNICAP RESURFACING PROSTHESIS

    FDA Adverse Event
    Other ·ARTHROSURFACE, INC.·Product code HSD·December 7, 2012

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MPRI·Product code DTB·April 10, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·April 4, 2011

    QUICKSITE LV

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008