BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    VITEK®2

    DI: 03573026555504 · Model: 9.01.0 · BIOMERIEUX , INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    VITEK®2
    Primary DI
    03573026555504
    Version / Model
    9.01.0
    Company Name
    BIOMERIEUX , INC.
    Labeler DUNS
    086785110
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2018-12-07
    Public Version
    4
    Public Version Date
    2023-08-03
    Public Version Status
    Update
    Public Device Record Key
    4aec6f19-93f8-414c-955a-9596387c1751
    Distribution End Date
    2020-06-03

    Device Description

    VITEK®2 software 9.01.0, advanced software to run your VITEK®2 system

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    LON SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION

    GMDN Terms

    Code Name
    56747 Microorganism identification/antimicrobial-susceptibility analyser IVD

    Identifiers

    Type ID
    Primary 03573026555504

    Premarket Submissions

    Submission Number Supplement Number
    N50510 082
    N50510 086