Pure Global

Quantitative Turbidimetric Immunoassay for Fibrinogen - India CDSCO Medical Device Registration

Quantitative Turbidimetric Immunoassay for Fibrinogen is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000021_f357a2b906c1decfba73e6d73a0113fc_9e6efb054b889567602731bd8b1b36fd. This device is marketed under the brand name Monospecific Coombs Serum. The license holder is TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is Sub Zonal Goa.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Quantitative Turbidimetric Immunoassay for Fibrinogen
UID: MFG/IVD/2021/000021_f357a2b906c1decfba73e6d73a0113fc_9e6efb054b889567602731bd8b1b36fd

Brand Name

Monospecific Coombs Serum

Device Class

Class C

Approving Authority

Sub Zonal Goa

Product Information

Quantia Fibrinogen is used in evaluating patients with a risk of atherosclerotic disease due to high fibrinogen levels. Low fibrinogen levels are observed in patients with liver disease, disseminated intravascular coagulation (Monospecific Coombs Serum)

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing