BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Arthrex®

    DI: 00888867212398 · Model: AR-8941PRS · ARTHREX, INC.
    View on AccessGUDID
    Product Codes
    3
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Arthrex®
    Primary DI
    00888867212398
    Version / Model
    AR-8941PRS
    Catalog Number
    AR-8941PRS
    Company Name
    ARTHREX, INC.
    Labeler DUNS
    131747628
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2017-02-15
    Public Version
    6
    Public Version Date
    2023-12-25
    Public Version Status
    Update
    Public Device Record Key
    57136d16-9df8-4623-b820-004da0e16ae5

    Device Description

    PLANTAR LAPIDUS PLATE, SHORT RIGHT

    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
    MR Conditional
    Direct Marking Exempt
    No
    PM Exempt
    No
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    Yes
    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
    HRS Plate, fixation, bone
    JDR Staple, fixation, bone
    HWC Screw, fixation, bone

    GMDN Terms

    Code Name
    46647 Orthopaedic fixation plate, non-bioabsorbable

    Identifiers

    Type ID
    Primary 00888867212398
    Secondary M150AR8941PRS1

    Customer Contacts

    Phone
    +1(800)934-4404
    Email
    [email protected]