BEUDAMED
    948 results · 22ms · Sources: EU EUDAMED, US FDA

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    CINCH QR SGW EXTENSION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PKIT, AXIS, LPV, SG, W/TUBING

    FDA UDI
    MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430114960·

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS LLC (PR)·Product code NIQ·April 27, 2005

    EXTRA BACK-UP 3.5

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DYB·April 27, 2005

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS LLC (PR)·Product code NIQ·April 27, 2005

    PKIT, AXIS, 5 IN. GT, SG, W/TUBING

    FDA UDI
    MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430114243·

    SHINOBI SGW

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DQX·March 22, 2010

    ATW GUIDEWIRE

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code DQX·September 26, 2012

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268108424·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268100541·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268110083·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268109698·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268109667·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268101173·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268109650·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268101227·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268100824·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268100831·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268100763·Guidewire

    Guidewire

    FDA UDI
    GALT MEDICAL CORP.·00841268100619·Guidewire