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

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    TIMX LOW BACK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984348·anteriors; shade B3; mould 92 S

    MODIFIED JELTRODE(TM) ELECTRODES DEEMED

    FDA 510(k)
    FDA Class 2 ·Neurology

    CUI FEATHERED SILICONE MALAR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GORE EXCLUDER AAA PROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES·Product code MIH·February 22, 2012

    ATLAS II PLUS HF CRT-D

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·February 28, 2013

    UNICEL® DXC 600 PRO SYNCHRON® CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·February 10, 2011

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·August 6, 2014