BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    PRINCETON

    DI: 00810158218765 · Model: 51291-00 · Princeton Medical Group, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    PRINCETON
    Primary DI
    00810158218765
    Version / Model
    51291-00
    Company Name
    Princeton Medical Group, Inc.
    Labeler DUNS
    012857277
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2026-02-05
    Public Version
    1
    Public Version Date
    2026-02-13
    Public Version Status
    New
    Public Device Record Key
    d9b04c55-a120-4d09-a41c-168a5c7c529c

    Device Description

    CANNULA LARYNGEAL 2.5MMØ WITH LUER-LOCK ATTACHMENT

    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
    Yes
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    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
    MDM Instrument, Manual, Surgical, General Use

    GMDN Terms

    Code Name
    10575 Lacrimal procedural cannula

    Identifiers

    Type ID
    Primary 00810158218765