BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Bausch + Lomb

    DI: 00757770058136 · Model: BL5420W · Bausch & Lomb Incorporated
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    6

    Basic Information

    Brand Name
    Bausch + Lomb
    Primary DI
    00757770058136
    Version / Model
    BL5420W
    Catalog Number
    BL5420W
    Company Name
    Bausch & Lomb Incorporated
    Labeler DUNS
    196603781
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    6
    Record Status
    Published
    Publish Date
    2016-11-07
    Public Version
    5
    Public Version Date
    2018-10-29
    Public Version Status
    Update
    Public Device Record Key
    68b224ae-0170-401b-91fe-708aa41834b4

    Device Description

    20ga Posterior Vitrectomy Pack with AFI and Wide Field Illuminator

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    Yes
    Over the Counter (OTC)
    No
    Kit
    Yes
    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
    No
    Has Expiration Date
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

    GMDN Terms

    Code Name
    47130 Vitrectomy fluid/gas handling handpiece/cannula

    Identifiers

    Type ID
    Primary 00757770058136
    Unit of Use 20757770058130