GUDIDData
eudamed_udi Primary ID: 06925794593559

ZINC REAGENT KIT(COLORIMETRIC METHOD) (UDI 06925794593559)

Manufactured by DIRUI INDUSTRIAL CO., LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZINC REAGENT KIT(COLORIMETRIC METHOD) - Primary ID 06925794593559

Device Regulatory Overview

The ZINC REAGENT KIT(COLORIMETRIC METHOD) (Model/Catalog Number: 3021693) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01010233 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
3021693
Product Code / EMDN
W01010233
Device Name
ZINC REAGENT KIT(COLORIMETRIC METHOD)
Database Sync Date
2026-08-09 18:07:26

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of ZINC REAGENT KIT(COLORIMETRIC METHOD)?

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

What is the Primary UDI-DI identifier for ZINC REAGENT KIT(COLORIMETRIC METHOD)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06925794593559.

What classification code is assigned to this device?

This device is registered under product classification code W01010233.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint