BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Kendall

    DI: 90884521148136 · Model: MI00325 · Cardinal Health, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    100

    Basic Information

    Brand Name
    Kendall
    Primary DI
    90884521148136
    Version / Model
    MI00325
    Catalog Number
    MI00325
    Company Name
    Cardinal Health, Inc.
    Labeler DUNS
    080935429
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    100
    Record Status
    Published
    Publish Date
    2016-09-24
    Public Version
    8
    Public Version Date
    2021-02-19
    Public Version Status
    Update
    Public Device Record Key
    8d6a284a-8ecb-4b44-aeea-5e52e1b02086

    Device Description

    3000 Isolation Chamber,Rectal

    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
    Primary 90884521148136
    Unit of Use 90884521535950

    Customer Contacts

    Phone
    +1(508)261-8000
    Email
    [email protected]

    Storage Conditions

    Type
    Special Storage Condition, Specify
    Special Conditions
    ;