BEUDAMED
    FDA Registration Active 🇳🇱 Netherlands

    PUREVIEW, ACTIVE LAPAROSCOPIC PLUME FILTRATION DEVICE

    Reg #: 3008837339 · FEI: 3008837339 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    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

    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
    Tubing/Tubing With Filter, Insufflation, Laparoscopic NKC

    Proprietary Names

    PUREVIEW, ACTIVE LAPAROSCOPIC PLUME FILTRATION DEVICE US ADAPTOR FOR UNIVERSAL GAS CONNECTION 16-L INSUFFLATOR TUBING HIGH FLOW INSUFFLATOR TUBING DISS ADAPTOR FOR UNIVERSAL GAS CONNECTION

    Establishment Types

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