BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    N/A

    DI: 04961333241187 · Model: 82171 · PENTAX OF AMERICA, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    25

    Basic Information

    Brand Name
    N/A
    Primary DI
    04961333241187
    Version / Model
    82171
    Company Name
    PENTAX OF AMERICA, INC.
    Labeler DUNS
    083211284
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    25
    Record Status
    Published
    Publish Date
    2018-03-13
    Public Version
    3
    Public Version Date
    2019-04-23
    Public Version Status
    Update
    Public Device Record Key
    f84f5061-c489-4f36-8b0c-1566b73a4d2e

    Device Description

    ELECTRODE,BIPOLAR PATIENT PAD, BOX= 25 P

    Device Characteristics

    Single Use
    Yes
    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
    No
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    GEI Electrosurgical, Cutting & Coagulation & Accessories

    GMDN Terms

    Code Name
    57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

    Identifiers

    Type ID
    Primary 04961333241187
    Unit of Use 14961333241184

    Premarket Submissions

    Submission Number Supplement Number
    K884836 000