Fibrin/Fibrinogen Degradation Products(FDP) Detection Kit(CLIA) (UDI 06974674893296)
Manufactured by Shenzhen Zijian Biotechnology Co., Ltd
Device Regulatory Overview
The Fibrin/Fibrinogen Degradation Products(FDP) Detection Kit(CLIA) (Model/Catalog Number: 18-02-0201) is a medical device manufactured by Shenzhen Zijian Biotechnology Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0103020502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 18-02-0201
- Product Code / EMDN
- W0103020502
- Device Name
- Fibrin/Fibrinogen Degradation Products(FDP) Detection Kit(CLIA)
- Database Sync Date
- 2026-08-09 16:59:31
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 Fibrin/Fibrinogen Degradation Products(FDP) Detection Kit(CLIA)?
The registered manufacturer of record for Fibrin/Fibrinogen Degradation Products(FDP) Detection Kit(CLIA) is Shenzhen Zijian Biotechnology Co., Ltd.
What is the Primary UDI-DI identifier for Fibrin/Fibrinogen Degradation Products(FDP) Detection Kit(CLIA)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974674893296.
What classification code is assigned to this device?
This device is registered under product classification code W0103020502.
Similar Classification Devices (W0103020502)
Other Devices by Shenzhen Zijian Biotechnology Co., Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint