BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Cranial Fusion

    FDA UDI
    Life Spine, Inc.·00190837085377·

    DENTA SAFE LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    AUTOGENESIS(TM) AUTOMATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALARIS PRIMARY TUBING

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·January 4, 2013

    LINA LOOP

    FDA Adverse Event
    Malfunction ·LINA MEDICAL POLSKA SP. Z.O.O·Product code KNF·December 16, 2010

    ENDO ILS, 29MM, CURVED

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 15, 2014