BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    E-Pacer

    DI: 00858101008292 · Model: K660 · RIFTON EQUIPMENT
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    E-Pacer
    Primary DI
    00858101008292
    Version / Model
    K660
    Company Name
    RIFTON EQUIPMENT
    Labeler DUNS
    808251438
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-09-13
    Public Version
    1
    Public Version Date
    2022-09-21
    Public Version Status
    New
    Public Device Record Key
    b48d70a5-d821-4ee6-9be6-7f6ecc0e9559

    Device Description

    Powered gait trainer and transfer device

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    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
    Yes
    Has Serial Number
    No
    Has Lot/Batch Number
    No
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    FSA Lift, Patient, Non-Ac-Powered

    GMDN Terms

    Code Name
    63674 Gait rehabilitation electronic walker

    Identifiers

    Type ID
    Primary 00858101008292

    Customer Contacts

    Phone
    800.571.8198
    Email
    [email protected]