BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    GlideScope®

    DI: 00879123006752 · Model: GlideScope® Core™ Smart Cable · Verathon Medical (Canada) ULC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    GlideScope®
    Primary DI
    00879123006752
    Version / Model
    GlideScope® Core™ Smart Cable
    Catalog Number
    0600-0783
    Company Name
    Verathon Medical (Canada) ULC
    Labeler DUNS
    243738320
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-12-08
    Public Version
    1
    Public Version Date
    2022-12-16
    Public Version Status
    New
    Public Device Record Key
    5adde4fc-fea5-4b97-847b-9b6baba1d5dc

    Device Description

    GlideScope® Core™ Smart Cable

    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
    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
    CCW Laryngoscope, Rigid

    GMDN Terms

    Code Name
    47487 Electrical-only medical device connection cable, reusable

    Identifiers

    Type ID
    Package 10879123006759
    Primary 00879123006752