BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    URIC ACID REAGENT (PROCEDURE NUMBER 686)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198260·AK3 PS Insert Trial Size 4, 16mm

    TRILOGY 200 VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Cellvizio I.V.E. with Confocal Miniprobes

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

    TRILOGY 200

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code CBK·August 19, 2020

    AUTOSOFT XC

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·June 22, 2024

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·November 5, 2010

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·February 11, 2014

    PUMP MMT-522NAS PRDGM INS V2.2 SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code CGA·July 9, 2008

    AUTOSOFT XC

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·June 22, 2024