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Chagas IgG Antibody Rapid Test - India CDSCO Medical Device Registration

Chagas IgG Antibody Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000113_d7b957ae5db1168a559f818e715acd19_d2e5c775775fc6281f827b95fb57d503. This device is marketed under the brand name Chimera. The license holder is CHIMERA BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is South Delhi 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
Chagas IgG Antibody Rapid Test
UID: MFG/IVD/2023/000113_d7b957ae5db1168a559f818e715acd19_d2e5c775775fc6281f827b95fb57d503

Brand Name

Chimera

Device Class

Class B

Approving Authority

South Delhi Division

Product Information

The Chimeraยฎ Chagas antibody Rapid Test is a rapid immunochromatographic strip assay for the qualitative detection of human lgG antibodies to Trypanosoma cruzi (Chimera) in human serum and whole blood

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