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UREA-B KIT - India CDSCO Medical Device Registration

UREA-B KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000005_fbd98f76b983e7931363003fc88528ef_cb32e79db203ce518c4a8a12731fb15a. This device is marketed under the brand name Lp-PLA2 Reagent. The license holder is M/s. Agappe Diagnostics Ltd., and it is classified as Device Class Class B. The approving authority is Kerala.

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
UREA-B KIT
UID: MFG/IVD/2020/000005_fbd98f76b983e7931363003fc88528ef_cb32e79db203ce518c4a8a12731fb15a

Brand Name

Lp-PLA2 Reagent

Device Class

Class B

Approving Authority

Kerala

Product Information

Diagnostic Device for the quantitative In-Vitro determination of Urea-B in human serum

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