CDSCO UID MFG/IVD/2021/000021_e586701d93ddbf5f2b9a8d74e0fa2b94_67a5382812fe804fe2c805b9a463c892

Fibrinogen determination Test

Name: Fibrinogen determination Test — CDSCO UID MFG/IVD/2021/000021_e586701d93ddbf5f2b9a8d74e0fa2b94_67a5382812fe804fe2c805b9a463c892
Creator: TULIP DIAGNOSTICS PRIVATE LIMITED
Keywords: Fibrinogen determination Test , MFG/IVD/2021/000021_e586701d93ddbf5f2b9a8d74e0fa2b94_67a5382812fe804fe2c805b9a463c892, Monospecific Coombs Serum, Device Class Class C, TULIP DIAGNOSTICS PRIVATE LIMITED, CDSCO registration

TULIP DIAGNOSTICS PRIVATE LIMITEDDevice Class Class CIndia CDSCOBrand: Monospecific Coombs Serum

VerifiedCDSCO · official registry

Registration details

UID: MFG/IVD/2021/000021_e586701d93ddbf5f2b9a8d74e0fa2b94_67a5382812fe804fe2c805b9a463c892
Device class: Class C
Brand name: Monospecific Coombs Serum
License holder: TULIP DIAGNOSTICS PRIVATE LIMITED
Approving authority: Sub Zonal Goa
Product information: Fibroquant is a reagent used for the quantitative estimation of Fibrinogen in plasma

About this record

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.

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