BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Phadia 5000E

    DI: 07333066020907 · Model: 12-4000-01 · Phadia AB
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Phadia 5000E
    Primary DI
    07333066020907
    Version / Model
    12-4000-01
    Catalog Number
    12-4000-01
    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
    c27abca1-b237-4683-98fc-bd43f3a49430

    Device Description

    Phadia 5000E

    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 07333066020907

    Customer Contacts

    Phone
    +469999999999
    Email
    [email protected]