GUDIDData
eudamed_udi Primary ID: 06942202260391

CHLORIDE REAGENT KIT (THIOCYANATE METHOD) (UDI 06942202260391)

Manufactured by DIRUI INDUSTRIAL CO., LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHLORIDE REAGENT KIT (THIOCYANATE METHOD) - Primary ID 06942202260391

Device Regulatory Overview

The CHLORIDE REAGENT KIT (THIOCYANATE METHOD) (Model/Catalog Number: 3021201) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01010299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
3021201
Product Code / EMDN
W01010299
Device Name
CHLORIDE REAGENT KIT (THIOCYANATE METHOD)
Database Sync Date
2026-08-09 16:29:08

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 CHLORIDE REAGENT KIT (THIOCYANATE METHOD)?

The registered manufacturer of record for CHLORIDE REAGENT KIT (THIOCYANATE METHOD) is DIRUI INDUSTRIAL CO., LTD.

What is the Primary UDI-DI identifier for CHLORIDE REAGENT KIT (THIOCYANATE METHOD)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942202260391.

What classification code is assigned to this device?

This device is registered under product classification code W01010299.

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