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Uric Acid testing kit - India CDSCO Medical Device Registration

Uric Acid testing kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000049_540be7328e5a89f7f43157d2063339a6_dd2e671dd5ed4b48fba0d054f015131e. This device is marketed under the brand name PROLISA T4 ELISA. The license holder is Promea Therapeutics Private Limited, and it is classified as Device Class Class B. The approving authority is Telangana.

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
Uric Acid testing kit
UID: MFG/IVD/2021/000049_540be7328e5a89f7f43157d2063339a6_dd2e671dd5ed4b48fba0d054f015131e

Brand Name

PROLISA T4 ELISA

Device Class

Class B

Approving Authority

Telangana

Product Information

The intended use of the kit is to solely detect the level of uric acid concentration in human serum or plasma

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