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    FDA UDI In Commercial Distribution 🇺🇸 United States

    Treatment Pack (Size L)

    DI: 04049471110067 · Model: 1462-334 · Carl Zeiss Meditec AG
    View on AccessGUDID
    Product Codes
    2
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    10

    Basic Information

    Brand Name
    Treatment Pack (Size L)
    Primary DI
    04049471110067
    Version / Model
    1462-334
    Company Name
    Carl Zeiss Meditec AG
    Labeler DUNS
    314594680
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    10
    Record Status
    Published
    Publish Date
    2016-09-23
    Public Version
    3
    Public Version Date
    2018-11-23
    Public Version Status
    Update
    Public Device Record Key
    1230a7b5-d0c1-4574-af43-e5d0dd4b7290

    Device Description

    single use patient interface for VisuMax laser keratome

    Device Characteristics

    Single Use
    Yes
    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
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    HQF Laser, Ophthalmic
    HNO Keratome, Ac-Powered

    GMDN Terms

    Code Name
    57995 Femtosecond ophthalmic solid-state laser system

    Identifiers

    Type ID
    Primary 04049471110067
    Unit of Use 04049471100068

    Device Sizes

    Type Value Unit Text
    Weight 400 Gram
    Device Size Text, specify LxWxH:260mmx160mmx100mm