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Creatinine Reagent Kit - India CDSCO Medical Device Registration

Creatinine Reagent Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000063_df709c23a914180a03651f080a6a35f0_498782ca38fba3b599782fcf7a0ae3d6. The license holder is Kee Diagnostics Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is South West Delhi 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
Creatinine Reagent Kit
UID: MFG/IVD/2020/000063_df709c23a914180a03651f080a6a35f0_498782ca38fba3b599782fcf7a0ae3d6

Device Class

Class B

Approving Authority

South West Delhi Division

Product Information

For the use of Quantitative determination of Creatinine in serum/plasma or urine

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