BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    Kendall

    DI: 20884527015587 · Model: 20550 · Cardinal Health, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    3
    Pkg Device Count
    2

    Basic Information

    Brand Name
    Kendall
    Primary DI
    20884527015587
    Version / Model
    20550
    Catalog Number
    20550
    Company Name
    Cardinal Health, Inc.
    Labeler DUNS
    080935429
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    2
    Record Status
    Published
    Publish Date
    2014-09-18
    Public Version
    10
    Public Version Date
    2023-07-03
    Public Version Status
    Update
    Public Device Record Key
    6f6a91af-e6b6-4aca-8365-2f6e2b355dfa
    Distribution End Date
    2023-07-01

    Device Description

    20550 Adult Multi-Function Defibrillation Electrodes,Radiotransparent

    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
    DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

    GMDN Terms

    Code Name
    11130 Electrode conductive skin pad, single-use

    Identifiers

    Type ID
    Package 10884527015580
    Primary 20884527015587
    Unit of Use 10884521264212

    Customer Contacts

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