BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    COILED TUBING 8FT, PACK 1

    Reg #: 3033536319 · FEI: 3033536319 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    12
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    MEDI.PLAN GMBH & CO. KG
    Registration Number
    3033536319
    FEI Number
    3033536319
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Hofkerstrabe 22
    City
    Dortmund
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K070060

    Owner / Operator

    Firm Name
    MEDI.PLAN GmbH & Co. KG
    Operator Number
    10091549
    Address
    Hofkerstrabe 24
    City
    Dortmund
    State
    DE-NOTA
    Postal Code
    44149
    Country
    DE
    Correspondent
    Amela Karic

    US Agent

    Business Name
    Capote Law Firm
    Contact Name
    Lisa Capote
    Address
    13818 SW 152nd Street, Suite 375
    City
    Miami
    State
    FL
    ZIP
    33177
    Country
    US
    Email
    [email protected]
    Phone
    786 8715680

    Products

    Device Name Product Code
    Blood Pressure Cuff DXQ

    Proprietary Names

    COILED TUBING 8FT, PACK 1 FLEXIPORT BP CUFF REUSABLE 1TB 25-34CM, LONG ADULT PACK 1 FLEXIPORT BP CUFF REUSABLE 1TB, SMALL ADULT PACK 1 FLEXIPORT BP CUFF REUSABLE, SMALL ADULT PACK 1 FLEXIPORT BP CUFF SINGLE USE, ADULT REGULAR PACK 20 FLEXIPORT BP CUFF SINGLE USE, ADULT LONG PACK 20 FLEXIPORT BP CUFF REUSABLE 2TB, SMALL ADULT PACK 1 FLEXIPORT BP CUFF REUSABLE 25-34CM, LONG ADULT PACK 1 FLEXIPORT BP CUFF REUSABLE, SMALL INFANT PACK 1 FLEXIPORT BP CUFF REUSABLE 25-34CM, ADULT PACK 1 FLEXIPORT BP CUFF REUSABLE 2TB 25-34CM, ADULT PACK 1 FLEXIPORT BP CUFF REUSABLE, INFANT PACK 1

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device