BEUDAMED
    18 results · 21ms · Sources: EU EUDAMED, US FDA

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    System, Nuclear Magnetic Resonance Imaging

    FDA Pre-Market Approval
    FDA Class 2 ·MAGNISCAN 5000 MRI SYSTEM

    System, Nuclear Magnetic Resonance Imaging

    FDA Pre-Market Approval
    FDA Class 2 ·MAGNISCAN 5000 MRI SYSTEM

    Pro Advantage

    FDA UDI
    NATIONAL DISTRIBUTION & CONTRACTING, INC.·M220P8500932·Pro Advantage Electrode Foam 2 3/4 Round 4PK

    Analyzer, Medical Image

    FDA Pre-Market Approval
    FDA Class 2 ·QVCAD SYSTEM

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·FEMORAL INTRODUCER SHEATH AND HEMOSTASIS (FISH) DEVICE 5,6, AND 8 FRENCH

    NA

    FDA UDI
    Zimmer, Inc.·00889024195950·

    NA

    FDA UDI
    Zimmer, Inc.·00889024195943·

    CARDIOGUARD STRESS TEST MONITOR 4002

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Analyzer, Medical Image

    FDA Pre-Market Approval
    FDA Class 2 ·QVCAD System (Version 3.3)

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·FEMORAL INTRODUCER SHEATH AND HEMOSTASIS (FISH) DEVICE 5,6, AND 8 FRENCH

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·Femoral Introducer Sheath and Hemostasis(FISH) Device

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·FEMORAL INTRODUCER SHEATH & HEMOSTASIS (FISH) DEVICE

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·FEMORAL INTRODUCER SHEATH AND HEMOSTASIS DEVICE

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·FEMORAL INTRODUCER SHEATH & HEMOSTASIS DEVICE (FISH)

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·7F FISH-SP DEVICE

    SUMMIT DUOFIX TAP SZ5 STD OFF

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. - 1818910·Product code LPH·June 4, 2014

    APEX HOLE ELIM POSITIVE STOP; APEX HOLE ELIM POSITIVE STOP

    FDA Adverse Event
    Injury ·Product code MRA·November 29, 2012

    PUMP MMT-522LNAS PRDGM INS SK EN ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·September 27, 2010