BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    TOXOPLASMA GONDII IGG ELISA

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LinkBio Instrument

    FDA UDI
    Link Bio Corp·00810022402245·Guide Rod, Tibial Cone, D 12/120 L

    LinkBio Instrument

    FDA UDI
    Link Bio Corp·00810022402269·Guide Rod, Tibial Cone, D 16/120 L

    LinkBio Instrument

    FDA UDI
    Link Bio Corp·00810022402276·Guide Rod, Tibial Cone, D 18/120 L

    LinkBio Instrument

    FDA UDI
    Link Bio Corp·00810022402238·Guide Rod, Tibial Cone, D 10/120 L

    LinkBio Instrument

    FDA UDI
    Link Bio Corp·00810022402252·Guide Rod, Tibial Cone, D 14/120 L

    POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VISCO 360 Viscosurgical System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HRS·June 13, 2014

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 16, 2010

    ASR ACETABULAR IMPLANT 64

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·December 13, 2012