BEUDAMED
    FDA Registration Active 🇫🇷 France

    FULL ECHO® PRO

    Reg #: 9612445 · FEI: 3002807433 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    26
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    PRODIMED
    Registration Number
    9612445
    FEI Number
    3002807433
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    4 rue de l'Europe
    City
    NEUILLY-EN-THELLE Oise
    Country
    FR

    Regulatory Submissions

    510(k) Number
    K983604

    Owner / Operator

    Firm Name
    Laboratoire CCD
    Operator Number
    9019576
    Address
    36 rue Brunel, --
    City
    PARIS
    State
    FR-75
    Postal Code
    75017
    Country
    FR

    US Agent

    Business Name
    Emergo Global Representation LLC
    Contact Name
    Yong Sun
    Address
    2500 Bee Cave Rd., Bldg. 1, Ste. 300
    City
    Austin
    State
    TX
    ZIP
    78746
    Country
    US
    Email
    [email protected]
    Phone
    512 3279997

    Products

    Device Name Product Code
    Catheter, Assisted Reproduction MQF

    Proprietary Names

    FULL ECHO® PRO FRYDMAN®ULTRASOFT ECHO CLASSIC ULTRASOFT MOCK 18 CM CLASSIC ULTRASOFT 18 CM ECHOGYN® EMBRYOVIEW M MOCK 23 CM INVENTCATH ECO CLASSIC ULTRASOFT MOCK 23 CM FULL ECHO®23 CM ECHOGYN®EMBRYOVIEW M 23 CM FRYDMAN® CLASSIC 4.5 FRYDMAN® ULTRASOFT SHORT FRYDMAN® SET ULTRASOFT FRYDMAN ® SET ECHO WITH GUIDE FRYDMAN® CLASSIC 5.5 T.D.T.®SET STYLET FOR FRYDMAN® ULTRASOFT & FRYDMAN® ULTRASOFT echo ECHOGYN® EMBRYOVIEW M MOCK 18 CM CLASSIC ULTRASOFT 23 CM MOCK CATHETER FRYDMAN® MEMORY STANDARD ULTRASOFT FRYDMAN ® SET ECHO FRYDMAN ® SOFT WITH GUIDE ECHOGYN ® EMBRYOVIEW M 18 CM ULTRASOFT FRYDMAN ® SET MOCK ULTRASOFT FRYDMAN® SET AVEC WIH GUIDE ULTRASOFT FRYDMAN® SET MOCK ECHO

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)