BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Mammotome revolve

    Reg #: 3010339638 · FEI: 3010339638 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Devicor Medical Products, Inc. Warehouse/Distribution/Service Center
    Registration Number
    3010339638
    FEI Number
    3010339638
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    4750 Lake Forest Dr Ste 120
    City
    Blue Ash
    State
    OH
    ZIP
    45242
    Country
    US

    Regulatory Submissions

    510(k) Number
    K152989

    Owner / Operator

    Firm Name
    Devicor Medical Products, Inc.
    Operator Number
    10033297
    Address
    300 E-Business Way, Fifth Floor
    City
    Cincinnati
    State
    OH
    Postal Code
    45241
    Country
    US
    Correspondent
    Katrine M Austin

    Products

    Device Name Product Code
    Instrument, Biopsy KNW

    Proprietary Names

    Mammotome revolve

    Establishment Types

    Remanufacture Medical Device