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IgG Antibody detection ELISA kit - India CDSCO Medical Device Registration

IgG Antibody detection ELISA kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000017_fb9506d6ab76f33e39626b84b5dcd24c_327c2128e99ff6ba4daeb76d767ab75c. This device is marketed under the brand name Standard F TSH FIA. The license holder is SD Biosensor Healthcare Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Haryana.

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 B
IgG Antibody detection ELISA kit
UID: MFG/IVD/2020/000017_fb9506d6ab76f33e39626b84b5dcd24c_327c2128e99ff6ba4daeb76d767ab75c

Brand Name

Standard F TSH FIA

Device Class

Class B

Approving Authority

Haryana

Product Information

It is an Enzyme Linked Immunosorbent Assay for the detection of anti-dengue IgG in human serum or plasma

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