BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    STERILE 5 IN 1 CONNECTORS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KANDI-NUCLEAR MED. DATA ACQU.&INFO.

    FDA 510(k)

    'RAPID ONE' - PROPOXYPHENE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·November 13, 2012

    VANTAGE ANTERIOR FIXATION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWQ·May 23, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 25, 2015

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 25, 2015