BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Medi-Trace Cadence

    DI: 20192253017639 · Model: 22770PC · Cardinal Health 200, LLC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    3
    Pkg Device Count
    2

    Basic Information

    Brand Name
    Medi-Trace Cadence
    Primary DI
    20192253017639
    Version / Model
    22770PC
    Catalog Number
    22770PC
    Company Name
    Cardinal Health 200, LLC
    Labeler DUNS
    961027315
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    2
    Record Status
    Published
    Publish Date
    2021-07-29
    Public Version
    3
    Public Version Date
    2023-02-20
    Public Version Status
    Update
    Public Device Record Key
    50a5d379-9fdb-4884-9852-da86196bf3b0

    Device Description

    Medi-Trace Cadence Adult, Pre-Connect Defibrillation electrode (10 PR/PK) - ZOLL

    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
    MKJ Automated external defibrillators (non-wearable)

    GMDN Terms

    Code Name
    11130 Electrode conductive skin pad, single-use

    Identifiers

    Type ID
    Package 50192253017630
    Primary 20192253017639
    Unit of Use 10192253017632