BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    AESCULAP

    DI: 04046964582059 · Model: US323 · AESCULAP, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    AESCULAP
    Primary DI
    04046964582059
    Version / Model
    US323
    Catalog Number
    US323
    Company Name
    AESCULAP, INC.
    Labeler DUNS
    082594540
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-09-23
    Public Version
    5
    Public Version Date
    2020-01-15
    Public Version Status
    Update
    Public Device Record Key
    89e43230-13a6-49b3-84c0-075882ba9bad

    Device Description

    Forceps, 7 7/8", (200 mm), working length: 4", (100 mm), width: 0,70 mm

    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
    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
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

    GMDN Terms

    Code Name
    47848 Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

    Identifiers

    Type ID
    Primary 04046964582059

    Customer Contacts

    Phone
    +1(800)282-9000
    Email
    [email protected]