BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    mytaMed

    DI: B351707710 · Model: 7.07.71 · Mytamed, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Let the assistant research this device

    The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Brand Name
    mytaMed
    Primary DI
    B351707710
    Version / Model
    7.07.71
    Catalog Number
    7.07.71
    Company Name
    Mytamed, Inc.
    Labeler DUNS
    015903922
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2018-02-16
    Public Version
    4
    Public Version Date
    2025-07-08
    Public Version Status
    Update
    Public Device Record Key
    96750db7-7781-4c9d-846b-f248b7f0d525
    Distribution End Date
    2024-12-31

    Device Description

    Ostium Seeker, Maxillary

    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
    KAK Probe, Ent

    GMDN Terms

    Code Name
    47862 Abdominal/ENT/orthopaedic surgical probe, reusable

    Identifiers

    Type ID
    Primary B351707710