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Auto 3-part Hematology Analyzer - India CDSCO Medical Device Registration

Auto 3-part Hematology Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000458_0d090b2efdb5176fd5d6c04e871b0783_b5097e80b39a0e83a3e1f81bd5af2f26. This device is marketed under the brand name Wheisman. The license holder is FINOVA HEALTHCARE PRIVATE LIMITED, and it is classified as Device Class Class B. 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 B
Auto 3-part Hematology Analyzer
UID: IMP/IVD/2022/000458_0d090b2efdb5176fd5d6c04e871b0783_b5097e80b39a0e83a3e1f81bd5af2f26

Brand Name

Wheisman

Device Class

Class B

Approving Authority

CDSCO

Product Information

The AC 310 AUTO HEMATOL OGY ANALYZE Risa quantitative, automated hematology analyzer and 3-part differential counter for in Vitro Diagnostic Use in clinical laboratories.

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