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Typhoid IgG/IgM Rapid Test - India CDSCO Medical Device Registration

Typhoid IgG/IgM Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000059_5cfd1dfb634249e0dacd60c3617152e0_5ebbab87913a9a18dc073de5327ba6a3. This device is marketed under the brand name Typhoid IgG/IgM Rapid Test. The license holder is Dygnova Healthcare Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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
Typhoid IgG/IgM Rapid Test
UID: MFG/IVD/2023/000059_5cfd1dfb634249e0dacd60c3617152e0_5ebbab87913a9a18dc073de5327ba6a3

Brand Name

Typhoid IgG/IgM Rapid Test

Device Class

Class B

Approving Authority

Kokan Division

Product Information

The Typhoid IgG/IgM Rapid kit is a rapid, qualitative and differential test for the detection of salmonella Typhi (Typhoid IgG/IgM Rapid Test) in human serum, plasma or whole blood

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