BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Liko Original HighBack Sling™, Mod. 200

    DI: 00887761983205 · Model: 35200405 · Liko AB
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Liko Original HighBack Sling™, Mod. 200
    Primary DI
    00887761983205
    Version / Model
    35200405
    Company Name
    Liko AB
    Labeler DUNS
    354818510
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2020-06-10
    Public Version
    2
    Public Version Date
    2021-04-07
    Public Version Status
    Update
    Public Device Record Key
    a8de1555-7d1a-49a2-a9f4-e4af0d7a1b12

    Device Description

    Patient lifting system divided leg sling

    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
    33476 Patient lifting system divided leg sling

    Identifiers

    Type ID
    Primary 00887761983205

    Customer Contacts

    Phone
    +1(800)445-3730
    Email
    [email protected]