BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    RPM2 Rx

    DI: 00850023296290 · Model: 7 Size (01) · MEDHAB, LLC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    RPM2 Rx
    Primary DI
    00850023296290
    Version / Model
    7 Size (01)
    Catalog Number
    Shoe insole size 1 (women 9.0 to 10.5) (men 7.0 to 8.5)
    Company Name
    MEDHAB, LLC
    Labeler DUNS
    107660874
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2020-09-23
    Public Version
    2
    Public Version Date
    2020-11-30
    Public Version Status
    Update
    Public Device Record Key
    398cb280-5847-4b23-a880-7552d7ce3a28
    Distribution End Date
    2020-11-30

    Device Description

    footbed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider.

    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
    Yes
    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
    IKK System, Isokinetic Testing And Evaluation

    GMDN Terms

    Code Name
    61782 Pressure monitoring insole

    Identifiers

    Type ID
    Primary 00850023296290