Neoscreen hTSH EIA kit - India CDSCO Medical Device Registration

Neoscreen hTSH EIA kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000053_f984cebf81bda6608d23a8652123b8d2_ca2356d851866dd09345a206aabe0406. This device is marketed under the brand name Immunoreactive Tripsinogen. The license holder is Trivitron Healthcare Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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CDSCO Registered

Class Class C

Neoscreen hTSH EIA kit

UID: MFG/IVD/2020/000053_f984cebf81bda6608d23a8652123b8d2_ca2356d851866dd09345a206aabe0406

Brand Name

Immunoreactive Tripsinogen

License Holder

Trivitron Healthcare Pvt. Ltd

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

This Neoscreen hTSH EIA (Immunoreactive Tripsinogen) kit is for the quantitative determination of human thyrotropin (Immunoreactive Tripsinogen) in blood specimens dried on filter paper as a primary test for screening of babies for congenital hypothyroidism (Immunoreactive Tripsinogen). Monitoring of L-thyroxine replacement therapy can also be performed using this test, especially in cases when transportation of serum samples to the laboratory is difficult

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Neoscreen IRT EIA Kit

Brand: Immunoreactive Tripsinogen

Trivitron Healthcare Pvt. Ltd

Neoscreen hTSH EIA kit - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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