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Phosphorus test reagent/kit - India CDSCO Medical Device Registration

Phosphorus test reagent/kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000034_9b8f571834cdd029281bd7fa8d7ff546_ccac4860d72fbb4cbc3f511209731d3c. 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
Phosphorus test reagent/kit
UID: MFG/IVD/2019/000034_9b8f571834cdd029281bd7fa8d7ff546_ccac4860d72fbb4cbc3f511209731d3c

Brand Name

GPO-PAP

Device Class

Class B

Approving Authority

Telangana

Product Information

Estimation of inorganic phosphorus in serum plasma / urine

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