BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    eCordum Cardiac Monitor (eCordum CM)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HHM

    FDA UDI
    Oticon A/S·05707131341112·G200, BTE 13 PP 2.4G 105 C091 HHM

    ALEXIS LAPAROSCOPIC SYSTEM

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

    ZMR HIP SYSTEM KWZ-PROSTHESIS, HIP, CONSTRAINED, CEMENTED OR UNCEMENTED, METAL/POLYMER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ZENITH AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

    FDA Adverse Event
    Injury ·COOK INC.·Product code MIH·October 7, 2008

    HS III PROXIMAL SEAL SYTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR,LLC·Product code GEI·June 25, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·July 13, 2011

    C8701, S ALEXIS LAP SYS W/ KII FIOS 5/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code GCJ·November 14, 2016