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CRP LATEX - India CDSCO Medical Device Registration

CRP LATEX is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000072_f3c8ce45a961e412e7b19818f44d35db_5d8e62f7bff278b4eb8d4dc7c95f40e4. This device is marketed under the brand name Ultichem. The license holder is Yucca Diagnostics, and it is classified as Device Class Class B. The approving authority is Pune 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
CRP LATEX
UID: MFG/IVD/2022/000072_f3c8ce45a961e412e7b19818f44d35db_5d8e62f7bff278b4eb8d4dc7c95f40e4

Brand Name

Ultichem

License Holder

Yucca Diagnostics

Device Class

Class B

Approving Authority

Pune Division

Product Information

CRP Latex Test is used to measure the CRP in human serum qualitatively and quantitatively. CRP Latex Test is used for professional in vitro diagnostic use only

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