Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

FDP Assay kit CLIA

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
06974521004097
Basic UDI-DI Code
B-06974521004097
Reference
SUPM084072
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

This kit is used for Used for in vitro quantitative detection of Fibrin Degradation Products (FDP) in human plasma samples. Fibrin/Fibrinogen Degradation Products (FDP) are a general term for various degradation products produced by the dissolution of fibrin/fibrinogen in the blood under the action of plasmin[1]. FDP is the result of the action of the fibrinolytic system, the body stimulates the fibrinolytic system when sick, with the activation of a series of fibrinolytics, the hydrolysis of fibrinogen in the body generates FDP. When thrombosis occurs, the plasmin system is also activated, and the fibrinolytic monomer is degraded by plasmin to form a smaller fragment that is FDP. So FDP is not only one of the screening indicators of the activity of the plasmin system, but also a more sensitive experimental index when the in vivo coagulation system is secondary to fibrinolysis, often combined with D-dimer detection, Diagnosis of some clinical diseases due to coagulation and fibrinolytic imbalance[2].

CND Nomenclature Codes

Code Description
W0103020502 FIBRINOGEN DEGRADATION PRODUCTS

Similar Devices

Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).

View all