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Urea test reagent/kit - India CDSCO Medical Device Registration

Urea test reagent/kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000034_9298a8e32a1b7c1d7b464149eb83d945_bd6be1b62947d821d7d8d335f6ca38b1. This device is marketed under the brand name GPO-PAP. The license holder is ADI Diagnostics Pvt Ltd, 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
Urea test reagent/kit
UID: MFG/IVD/2019/000034_9298a8e32a1b7c1d7b464149eb83d945_bd6be1b62947d821d7d8d335f6ca38b1

Brand Name

GPO-PAP

Device Class

Class B

Approving Authority

Telangana

Product Information

Estimation of urea/blood urea nitrogen in plasma/serum/urine

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