BEUDAMED
    FDA Registration Active 🇵🇱 Poland

    Rapid-I Kit

    Reg #: 3007766601 · FEI: 3007766601 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    STERIPACK MEDICAL POLAND SP. Z O.O.
    Registration Number
    3007766601
    FEI Number
    3007766601
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Leg, ul. Japonska 1
    City
    Jelcz-Laskowice Dolnoslaskie
    Country
    PL

    Regulatory Submissions

    510(k) Number
    K181461

    Owner / Operator

    Firm Name
    SteriPack Medical Poland Sp. z o.o.
    Operator Number
    10029329
    Address
    Leg, ul. Japonska 1
    City
    Jelcz-Laskowice
    State
    PL-NOTA
    Postal Code
    55-220
    Country
    PL
    Correspondent
    Adam Sztaba

    US Agent

    Business Name
    SteriPack USA (Limited) LLC
    Contact Name
    Marinela Cebic
    Address
    4255 S Pipkin Rd
    City
    Lakeland
    State
    FL
    ZIP
    33811
    Country
    US
    Email
    [email protected]
    Phone
    863 6482333

    Products

    Device Name Product Code
    Labware, Assisted Reproduction MQK

    Proprietary Names

    Rapid-I Kit

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)