GUDIDData
eudamed_udi Primary ID: 06925794517623

D-Dimer Detection Kit (Latex Immunoturbidimetric Assay) (UDI 06925794517623)

Manufactured by DIRUI INDUSTRIAL CO., LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for D-Dimer Detection Kit (Latex Immunoturbidimetric Assay) - Primary ID 06925794517623

Device Regulatory Overview

The D-Dimer Detection Kit (Latex Immunoturbidimetric Assay) (Model/Catalog Number: 3009965) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W0103020503 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
3009965
Product Code / EMDN
W0103020503
Device Name
D-Dimer Detection Kit (Latex Immunoturbidimetric Assay)
Database Sync Date
2026-08-09 16:29:40

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of D-Dimer Detection Kit (Latex Immunoturbidimetric Assay)?

The registered manufacturer of record for D-Dimer Detection Kit (Latex Immunoturbidimetric Assay) is DIRUI INDUSTRIAL CO., LTD.

What is the Primary UDI-DI identifier for D-Dimer Detection Kit (Latex Immunoturbidimetric Assay)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06925794517623.

What classification code is assigned to this device?

This device is registered under product classification code W0103020503.

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