BEUDAMED
    FDA Registration Active 🇳🇱 Netherlands

    Target Helical Ultra

    Reg #: 3008837339 · FEI: 3008837339 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    11
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    STRYKER EMEA Supply Chain Services
    Registration Number
    3008837339
    FEI Number
    3008837339
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Frans Maasweg 2
    City
    Venlo Limburg
    Country
    NL

    Regulatory Submissions

    510(k) Number
    K123377

    Owner / Operator

    Firm Name
    STRYKER CORP.
    Operator Number
    1811755
    Address
    4100 East Milham Ave.
    City
    Kalamazoo
    State
    MI
    Postal Code
    49001
    Country
    US

    Products

    Device Name Product Code
    Device, Vascular, For Promoting Embolization KRD
    Device, Neurovascular Embolization HCG

    Proprietary Names

    Target Helical Ultra Target XL 360 Standard Target XL 3D Target 360 Ultra Target 3D Target Detachable Coil Target XL 360 Soft Target XL 360+ Target XL Helical Target 360 Soft Target 360+

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device