BEUDAMED
    FDA Registration Active 🇭🇺 Hungary

    Kolibri Percutaneous Nephrostomy Kits

    Reg #: 3003814961 · FEI: 3003814961 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    COLOPLAST HUNGARY KFT
    Registration Number
    3003814961
    FEI Number
    3003814961
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    BUZAVIRAG UT 15
    City
    TATABANYA Komarom-Esztergom
    Country
    HU

    Regulatory Submissions

    510(k) Number
    K211911

    Owner / Operator

    Firm Name
    Coloplast Corp.
    Operator Number
    8010144
    Address
    1601 West River Road North
    City
    Minneapolis
    State
    MN
    Postal Code
    55411
    Country
    US

    US Agent

    Business Name
    COLOPLAST CORP.
    Contact Name
    Jason Woehrle
    Address
    1601 West River Road N
    City
    Minneapolis
    State
    MN
    ZIP
    55411
    Country
    US
    Email
    [email protected]
    Phone
    612 7302063

    Products

    Device Name Product Code
    Stent, Ureteral FAD
    Catheter, Nephrostomy LJE

    Proprietary Names

    Kolibri Percutaneous Nephrostomy Kits Kolibri Direct Puncture Sets Kolibri Percutaneous Nephrostomy Catheters

    Establishment Types

    Repack or Relabel Medical Device