BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    CRANIALMAP

    DI: 07613252510949 · Model: 81-81031 · Stryker Leibinger GmbH & Co. KG
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    CRANIALMAP
    Primary DI
    07613252510949
    Version / Model
    81-81031
    Catalog Number
    81-81031
    Company Name
    Stryker Leibinger GmbH & Co. KG
    Labeler DUNS
    316153956
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-08-24
    Public Version
    2
    Public Version Date
    2018-03-29
    Public Version Status
    Update
    Public Device Record Key
    53241447-495b-4798-8426-7481f4fa953a

    Device Description

    CRANIALMAP(TM) EXPRESS SALES DEMO

    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
    HAW Neurological stereotaxic Instrument

    GMDN Terms

    Code Name
    42895 Robotic surgical navigation system application software

    Identifiers

    Type ID
    Primary 07613252510949