BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

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    TITANIUM ALLOY BONE SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970549·anteriors; shade BL3; mould UIM

    TOKUYAMA CUREGRACE

    FDA 510(k)
    FDA Class 2 ·Dental

    STRAUMANN P.004 RC GOLD ABUTMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    SEE H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

    DUETTE MULTI-BAND MUCOSECTOMY DEVICE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code KOG·July 3, 2014

    PROFEMUR(R) Z STEM PLASMA SPRAYED

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·February 20, 2013

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 25, 2011

    M2A-MAGNUM PF CUP 54ODX48ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 31, 2014

    CERAMIC ELECTRODE TIP L-HK F/GK372R

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code GEI·July 5, 2019