BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    KineMatch® PFR System

    DI: 00818720011257 · Model: Custom 102 · Kinamed, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    KineMatch® PFR System
    Primary DI
    00818720011257
    Version / Model
    Custom 102
    Catalog Number
    Custom 102
    Company Name
    Kinamed, Inc.
    Labeler DUNS
    184896645
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2015-11-04
    Public Version
    4
    Public Version Date
    2020-04-13
    Public Version Status
    Update
    Public Device Record Key
    8209167f-0e55-4fd7-a308-878b616b7402

    Device Description

    Custom PFR Primary Right

    Device Characteristics

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

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    KRR PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

    GMDN Terms

    Code Name
    58227 Patellofemoral joint prosthesis

    Identifiers

    Type ID
    Primary 00818720011257