BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Curaplex®

    DI: 00810094578411 · Model: FGIVBLOOD02-25-KIT · BOUND TREE MEDICAL, LLC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    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
    Curaplex®
    Primary DI
    00810094578411
    Version / Model
    FGIVBLOOD02-25-KIT
    Catalog Number
    FGIVBLOOD02-25-KIT
    Company Name
    BOUND TREE MEDICAL, LLC
    Labeler DUNS
    070556204
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2025-07-09
    Public Version
    1
    Public Version Date
    2025-07-17
    Public Version Status
    New
    Public Device Record Key
    cebcad1b-3d39-4ecc-9bd9-c11d90b28f1d

    Device Description

    Curaplex Buddy Blood Kit

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    No
    Kit
    Yes
    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
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    JKA Tubes, vials, systems, serum separators, blood collection

    GMDN Terms

    Code Name
    31336 Arterial blood sampling kit

    Identifiers

    Type ID
    Package 00810094579302
    Primary 00810094578411