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

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    AUTOSTAT II ANTI-GLIADIN IGA ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993086·anteriors; shade A3; mould UCM

    TUBE GASTROSTOMY

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ARTHROSTEER ABLATOR & COAGULATOR, MODELS: REF 1070 & 1080

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

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·March 1, 2013

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·August 8, 2014

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·February 8, 2011