COVID SCREEN PLUS ELISA kit - India CDSCO Medical Device Registration

COVID SCREEN PLUS ELISA kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000053_aa8e1118d8bb085b6dd98882f0e3f02f_4b83317130ac81723dc47d156e58e845. 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

COVID SCREEN PLUS ELISA kit

UID: MFG/IVD/2020/000053_aa8e1118d8bb085b6dd98882f0e3f02f_4b83317130ac81723dc47d156e58e845

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

A sensitive enzyme linked immunosorbent assay for the qualitative detection of IgG IgM, IgA antibodies to novel Covid – 19 (Immunoreactive Tripsinogen) in Human Serum or Plasma The kit is basically intended to screen samples to identify the infected units of blood and for clinical diagnostic testing

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Neoscreen IRT EIA Kit

Brand: Immunoreactive Tripsinogen

Trivitron Healthcare Pvt. Ltd

COVID SCREEN PLUS ELISA kit - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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