BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Jenx (Daytot)

    DI: 05056235223221 · Model: 207-605 · JENX LIMITED
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    Jenx (Daytot)
    Primary DI
    05056235223221
    Version / Model
    207-605
    Company Name
    JENX LIMITED
    Labeler DUNS
    291659639
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2025-08-08
    Public Version
    1
    Public Version Date
    2025-08-18
    Public Version Status
    New
    Public Device Record Key
    ac1cf710-f80c-40ab-86ec-9df43a571fc4

    Device Description

    Joey Size 2 Wipe Clean

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    Yes
    Not Made with NRL
    No
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    Yes
    Has Serial Number
    Yes
    Has Lot/Batch Number
    No
    Has Manufacturing Date
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    CCX Support, Patient Position

    GMDN Terms

    Code Name
    31166 Assistive crawler/mobility board

    Identifiers

    Type ID
    Primary 05056235223221