BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Reprocessed LigaSure Maryland Jaw Sealer/Divider

    Reg #: 3009350690 · FEI: 3009350690 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Stryker Sustainability Solutions
    Registration Number
    3009350690
    FEI Number
    3009350690
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1810 W. Drake Dr.
    City
    Tempe
    State
    AZ
    ZIP
    85283
    Country
    US

    Regulatory Submissions

    510(k) Number
    K180499

    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
    Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed NUJ
    Electrosurgical, Cutting & Coagulation & Accessories GEI

    Proprietary Names

    Reprocessed LigaSure Maryland Jaw Sealer/Divider

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility