BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    PRINCETON

    DI: 00810158215450 · Model: 71309-00 · 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
    00810158215450
    Version / Model
    71309-00
    Company Name
    Princeton Medical Group, Inc.
    Labeler DUNS
    012857277
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2025-06-10
    Public Version
    1
    Public Version Date
    2025-06-18
    Public Version Status
    New
    Public Device Record Key
    5691d460-afed-425f-8aee-b5cd369bcbaf

    Device Description

    SPECULUM AUVARD VAGINAL 105MM X 38MM WITH FIXED WEIGHT 1.4KG (3 LBS)

    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
    HDF Speculum, Vaginal, Metal

    GMDN Terms

    Code Name
    35352 Vaginal speculum, reusable

    Identifiers

    Type ID
    Primary 00810158215450