BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Kendall

    DI: 10884527022076 · Model: MK00175 · Cardinal Health, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Kendall
    Primary DI
    10884527022076
    Version / Model
    MK00175
    Catalog Number
    MK00175
    Company Name
    Cardinal Health, Inc.
    Labeler DUNS
    080935429
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-09-24
    Public Version
    9
    Public Version Date
    2023-06-01
    Public Version Status
    Update
    Public Device Record Key
    9a7b1367-7029-4c13-99e9-46c68f9b4087
    Distribution End Date
    2025-12-31

    Device Description

    3201P Apnea Products

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    Yes
    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
    GXY ELECTRODE, CUTANEOUS

    GMDN Terms

    Code Name
    35995 Transcutaneous electrical stimulation electrode, single-use

    Identifiers

    Type ID
    Package 90884527022072
    Primary 10884527022076

    Storage Conditions

    Type
    Special Storage Condition, Specify
    Special Conditions
    ;