BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Preciset RF

    DI: 04015630914531 · Model: 12172828322 · Roche Diagnostics GmbH
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Preciset RF
    Primary DI
    04015630914531
    Version / Model
    12172828322
    Catalog Number
    12172828322
    Company Name
    Roche Diagnostics GmbH
    Labeler DUNS
    315028860
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-09-20
    Public Version
    3
    Public Version Date
    2018-07-06
    Public Version Status
    Update
    Public Device Record Key
    465e7b99-0228-45bb-8ec6-ae4cf8a59c53

    Device Characteristics

    Single Use
    Yes
    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
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    DHR SYSTEM, TEST, RHEUMATOID FACTOR

    GMDN Terms

    Code Name
    30505 Plasma protein IVD, calibrator

    Identifiers

    Type ID
    Primary 04015630914531

    Premarket Submissions

    Submission Number Supplement Number
    K002609 000

    Storage Conditions

    Type
    Storage Environment Temperature
    Temperature Range
    2 – 8 Degrees Celsius