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Fibrinogen determination Test - India CDSCO Medical Device Registration

Fibrinogen determination Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000021_e586701d93ddbf5f2b9a8d74e0fa2b94_67a5382812fe804fe2c805b9a463c892. 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 determination Test
UID: MFG/IVD/2021/000021_e586701d93ddbf5f2b9a8d74e0fa2b94_67a5382812fe804fe2c805b9a463c892

Brand Name

Monospecific Coombs Serum

Device Class

Class C

Approving Authority

Sub Zonal Goa

Product Information

Fibroquant is a reagent used for the quantitative estimation of Fibrinogen in plasma

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