BEUDAMED
    FDA Registration Active 🇸🇪 Sweden

    ImmunoCAP Allergen e220, Allergen component rFel d 2 Cat serum albumin

    Reg #: 9610566 · FEI: 3002807876 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    12
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    PHADIA AB
    Registration Number
    9610566
    FEI Number
    3002807876
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    RAPSGATAN 7P
    City
    UPPSALA
    Country
    SE

    Regulatory Submissions

    510(k) Number
    K101251

    Owner / Operator

    Firm Name
    PHADIA AB
    Operator Number
    9004441
    Address
    Rapsgatan 7P, P.O. Box 6460
    City
    UPPSALA
    State
    SE-C
    Postal Code
    75137
    Country
    SE

    US Agent

    Business Name
    Phadia US Inc.
    Contact Name
    Carla Krause
    Address
    4169 Commercial Avenue
    City
    Portage
    State
    MI
    ZIP
    49002
    Country
    US
    Email
    [email protected]
    Phone
    616 2864138

    Products

    Device Name Product Code
    System, Test, Radioallergosorbent (Rast) Immunological DHB

    Proprietary Names

    ImmunoCAP Allergen e220, Allergen component rFel d 2 Cat serum albumin ImmunoCAP Allergen g216, Allergen component nCyn d 1 Bermuda grass ImmunoCAP Allergen f424, Allergen component rAra h 3 Peanut ImmunoCAP Allergen e94, Allergen component rFel d 1 Cat ImmunoCAP Allergen m229, Allergen component rAlt a 1, Alternaria alternata ImmunoCAP Allergen f352, Allergen component rAra h 8 PR-10, Peanut ImmunoCAP Allergen d203, Allergen component rDer p 2, House dust mite ImmunoCAP Allergen d205, Allergen component rDer p 10 Tropomyosin, House dust mite ImmunoCAP Allergen w230, Allergen component nAmb a 1 Ragweed ImmunoCAP Allergen f423, Allergen component rAra h 2 Peanut ImmunoCAP Allergen f422, Allergen component rAra h 1 Peanut ImmunoCAP Allergen f427, Allergen component rAra h 9 LTP, Peanut

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device