BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Lumbar Interbody Fusion System (OLLIF)

    DI: 00850014575670 · Model: 01-05 · ADVANCED RESEARCH MEDICAL LLC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Lumbar Interbody Fusion System (OLLIF)
    Primary DI
    00850014575670
    Version / Model
    01-05
    Catalog Number
    01-05
    Company Name
    ADVANCED RESEARCH MEDICAL LLC
    Labeler DUNS
    117201206
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2021-09-03
    Public Version
    1
    Public Version Date
    2021-09-13
    Public Version Status
    New
    Public Device Record Key
    72b6ab1e-8b2f-49b5-829f-079614b41dca

    Device Description

    Lumbar Interbody Fusion System (OLLIF) Pituitary Rongeur

    Device Characteristics

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    MAX Intervertebral Fusion Device With Bone Graft, Lumbar

    GMDN Terms

    Code Name
    35541 Spinal rongeur

    Identifiers

    Type ID
    Primary 00850014575670

    Customer Contacts

    Phone
    6124401865
    Email
    [email protected]

    Premarket Submissions

    Submission Number Supplement Number
    K173947 000