GUDIDData
eudamed_udi Primary ID: 06974674892268

ST2 FIA Kit (UDI 06974674892268)

Manufactured by Shenzhen Zijian Biotechnology Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ST2 FIA Kit - Primary ID 06974674892268

Device Regulatory Overview

The ST2 FIA Kit (Model/Catalog Number: 18-02-0056) is a medical device manufactured by Shenzhen Zijian Biotechnology Co., Ltd. This product is indexed under FDA Product Code / Category Classification W01021314 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
18-02-0056
Product Code / EMDN
W01021314
Device Name
ST2 FIA Kit
Database Sync Date
2026-08-09 16:50:08

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 ST2 FIA Kit?

The registered manufacturer of record for ST2 FIA Kit is Shenzhen Zijian Biotechnology Co., Ltd.

What is the Primary UDI-DI identifier for ST2 FIA Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974674892268.

What classification code is assigned to this device?

This device is registered under product classification code W01021314.

Programmatic Export

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

JSON API Endpoint