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Anti A - India CDSCO Medical Device Registration

Anti A is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000792_7ae85e40048d0cff3bca1f6edde700c6_e8a4d2d22d70fc732f2a63e934fc6e2a. This device is marketed under the brand name NOVACLONE Anti-A Murine Monoclonal. The license holder is Immucor India Pvt. Ltd.,, and it is classified as Device Class Class D. The approving authority is CDSCO.

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 D
Anti A
UID: IMP/IVD/2020/000792_7ae85e40048d0cff3bca1f6edde700c6_e8a4d2d22d70fc732f2a63e934fc6e2a

Brand Name

NOVACLONE Anti-A Murine Monoclonal

Device Class

Class D

Approving Authority

CDSCO

Product Information

NOVACLONE Anti-A Murine Monoclonal provides a specific qualitative test for the detection of human blood group antigen โ€“ A. The test used with these Blood Grouping Reagents is based on the principle of direct hemagglutination. Incubation of test red cells with NOVACLONEโ„ข Anti-A, Anti-B or Anti-A

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