BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO HYPERTRANSIT INFUSION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Modulus

    FDA UDI
    Nuvasive, Inc.·00887517968814·Modulus TLIF-A Inserter

    MEDISYSTEMS LUER ACCESS INJECTION SITE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    STAPLETAC2 BONE ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NV GXL LINR, NTRL, 32MM ID, GROUP 2 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code MEH·July 20, 2022

    NV GXL LNR, LIPPED, 36MM ID, GROUP 3 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·July 9, 2024

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code CBK·April 16, 2013

    HIRES 90K

    FDA Adverse Event
    Injury ·ADVANCED BIONICS LLC·Product code MCM·April 19, 2011

    2600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008

    NV GXL LINR, NTRL, 28MM ID, GROUP 1 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 11, 2024

    NV GXL LINR, NTRL, 36MM ID, GROUP 3 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 28, 2024