BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Phadia 5000E+E

    DI: 07333066020914 · Model: 12-4000-02 · Phadia AB
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Phadia 5000E+E
    Primary DI
    07333066020914
    Version / Model
    12-4000-02
    Catalog Number
    12-4000-02
    Company Name
    Phadia AB
    Labeler DUNS
    354019424
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2020-12-01
    Public Version
    3
    Public Version Date
    2023-12-11
    Public Version Status
    Update
    Public Device Record Key
    0329c35d-151c-4aab-b60b-8202ecb1ffd9

    Device Description

    Phadia 5000E+E

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    Yes
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    No
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    No
    Has Serial Number
    Yes
    Has Lot/Batch Number
    No
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    NHX ANTIBODIES, ANTI-CYCLIC CITRULLINATED PEPTIDE (CCP)

    GMDN Terms

    Code Name
    56705 Fluorescent immunoassay analyser IVD, laboratory

    Identifiers

    Type ID
    Primary 07333066020914

    Customer Contacts

    Phone
    +469999999999
    Email
    [email protected]