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Fibrinogen Control Level-I - India CDSCO Medical Device Registration

Fibrinogen Control Level-I is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000021_e2d10fc3f3c26fab87f93fdfb1693bab_8040116f1550459db820a43a093fd597. 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.

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CDSCO Registered
Class Class C
Fibrinogen Control Level-I
UID: MFG/IVD/2021/000021_e2d10fc3f3c26fab87f93fdfb1693bab_8040116f1550459db820a43a093fd597

Brand Name

Monospecific Coombs Serum

Device Class

Class C

Approving Authority

Sub Zonal Goa

Product Information

Seroquant range of controls are assayed controls useful for monitoring the precision of laboratory testing procedures. Seroquant controls are also useful for validating the calibration and performance of the respective reagents using a turbidimetry analyzer

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