BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    AESCULAP XENON LIGHT SOURCE

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

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984124·anteriors; shade A3; mould 93

    OMNIFIT SELF TAPPING CANCELLOUS BONE SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AUTOMATED EIA READER MODEL EL311

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SPIROBAC FILTER REINF MEMBRANE

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code CAH·August 1, 2012

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 28, 2013

    CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code DYE·February 10, 2011

    SUPER SUCKER SHORT CURVED (BX/20)

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code KDC·December 18, 2013