BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    GoLift

    DI: 00840722000069 · Model: GO-LIFT-400 · Amico Mobility Solutions Corporation
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    GoLift
    Primary DI
    00840722000069
    Version / Model
    GO-LIFT-400
    Catalog Number
    GO-LIFT-400
    Company Name
    Amico Mobility Solutions Corporation
    Labeler DUNS
    203776500
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2021-02-01
    Public Version
    2
    Public Version Date
    2021-03-23
    Public Version Status
    Update
    Public Device Record Key
    eba9aa2a-023d-45d7-bdaf-242fc40a7f4b

    Device Description

    GOLIFT 400LBS-AMICO (POWER SUPPLY EXCLUDED)

    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
    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
    FSA Lift, Patient, Non-Ac-Powered

    GMDN Terms

    Code Name
    38129 Overhead track patient lifting/transfer system

    Identifiers

    Type ID
    Primary 00840722000069

    Customer Contacts

    Phone
    (905) 764-0800
    Email
    [email protected]

    Storage Conditions

    Type
    Handling Environment Humidity
    Temperature Range
    20 – 90 Percent (%) Relative Humidity