BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Reprocessed DECANAV Electrophysiology Catheter

    Reg #: 3011276773 · FEI: 3011276773 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    STERILMED, INC.
    Registration Number
    3011276773
    FEI Number
    3011276773
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5010 Cheshire Pkwy N Ste 2
    City
    Plymouth
    State
    MN
    ZIP
    55446
    Country
    US

    Regulatory Submissions

    510(k) Number
    K240826

    Owner / Operator

    Firm Name
    STERILMED, INC.
    Operator Number
    9030419
    Address
    5010 Cheshire Parkway N, Suite 2
    City
    Plymouth
    State
    MN
    Postal Code
    55446
    Country
    US
    Correspondent
    Umar Malik

    Products

    Device Name Product Code
    Catheter, Recording, Electrode, Reprocessed NLH
    Catheter, Electrode Recording, Or Probe, Electrode Recording DRF

    Proprietary Names

    Reprocessed DECANAV Electrophysiology Catheter

    Establishment Types

    Reprocess Single-Use Device Develop Specifications But Do Not Manufacture At This Facility