BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    MaxMoreSpine

    DI: 04260200312532 · Model: 1001-BE 001/S · Hoogland Spine Products GmbH
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    MaxMoreSpine
    Primary DI
    04260200312532
    Version / Model
    1001-BE 001/S
    Company Name
    Hoogland Spine Products GmbH
    Labeler DUNS
    507292204
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-08-02
    Public Version
    1
    Public Version Date
    2022-08-10
    Public Version Status
    New
    Public Device Record Key
    833df84d-9f5d-4be6-9c52-ead982ac25c8

    Device Description

    Shaft for Bipoi. Handel Flex. Electrodem

    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
    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
    GEI Electrosurgical, Cutting & Coagulation & Accessories

    GMDN Terms

    Code Name
    32684 Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

    Identifiers

    Type ID
    Primary 04260200312532