Pure Global

Antinuclear Antibody Test - India CDSCO Medical Device Registration

Antinuclear Antibody Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000113_d76c3c40dde707ed811008cd58b30db9_fc3b2044a3c142d5c135b8880ae511ad. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Antinuclear Antibody Test
UID: MFG/IVD/2023/000113_d76c3c40dde707ed811008cd58b30db9_fc3b2044a3c142d5c135b8880ae511ad

Brand Name

Chimera

Device Class

Class B

Approving Authority

South Delhi Division

Product Information

The ANA Screen ELISA test system is an enzyme-linked immunosorbent assay (Chimera) for the detection of IgG class antibodies to ANA in human serum or plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing