Fibrin(ogen) Degradation Products (FDP) Assay Kit (lmmunoturbidimetry Method) (UDI 06903053025867)
Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Device Regulatory Overview
The Fibrin(ogen) Degradation Products (FDP) Assay Kit (lmmunoturbidimetry Method) (Model/Catalog Number: 105-029092-00) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics 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
- 105-029092-00
- Product Code / EMDN
- W0103020502
- Device Name
- Fibrin(ogen) Degradation Products (FDP) Assay Kit (lmmunoturbidimetry Method)、Fibrin(ogen) Degradation Products (FDP) Calibrators、Fibrin(ogen) Degradation Products (FDP) Control
- Database Sync Date
- 2026-08-09 17:27:55
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Fibrin(ogen) Degradation Products (FDP) Assay Kit (lmmunoturbidimetry Method)?
The registered manufacturer of record for Fibrin(ogen) Degradation Products (FDP) Assay Kit (lmmunoturbidimetry Method) is Shenzhen Mindray Bio-Medical Electronics Co., Ltd..
What is the Primary UDI-DI identifier for Fibrin(ogen) Degradation Products (FDP) Assay Kit (lmmunoturbidimetry Method)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06903053025867.
What classification code is assigned to this device?
This device is registered under product classification code W0103020502.
Similar Classification Devices (W0103020502)
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