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

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    VISITEC SILICONE RETINAL IMPLANTS/EXPLANTS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PCA(R) E SERIES HIP SYSTEM (CEMENTLESS USE)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EDGE COATED ELECTRODE

    FDA Adverse Event
    COVIDIEN VALLEYLAB·Product code GEI·November 22, 2010

    PINNACLE MTL INS NEUT44IDX62OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·July 18, 2014

    LOCK-NUT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·December 26, 2012