Neoscreen IRT EIA Kit - India CDSCO Medical Device Registration

Neoscreen IRT EIA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000053_fb967a5e52937e5fb92434bfb45e62c4_03f38ba9937025a28380fa272d64986b. 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.

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

Neoscreen IRT EIA Kit

UID: MFG/IVD/2020/000053_fb967a5e52937e5fb92434bfb45e62c4_03f38ba9937025a28380fa272d64986b

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

Labsystem Diagnostics Neoscreen IRT EIA test is a simple competition Enzyme immunoassay enabling the quantification of immunoreactive Trypsinogen present in blood samples dried on filter paper

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Neoscreen hTSH EIA kit

Brand: Immunoreactive Tripsinogen

Trivitron Healthcare Pvt. Ltd

Neoscreen IRT EIA Kit - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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