BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Reprocessed EP Catheter and Cable

    Reg #: 2090040 · FEI: 3002615969 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Stryker Sustainability Solutions Phoenix
    Registration Number
    2090040
    FEI Number
    3002615969
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    10232 S. 51st St.
    City
    Phoenix
    State
    AZ
    ZIP
    85044
    Country
    US

    Regulatory Submissions

    510(k) Number
    K030026

    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
    Catheter, Recording, Electrode, Reprocessed NLH
    Cable, Transducer And Electrode, Patient, (Including Connector) DSA

    Proprietary Names

    Reprocessed EP Catheter and Cable

    Establishment Types

    Reprocess Single-Use Device