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Creatinine Enzymatic Test Kit - India CDSCO Medical Device Registration

Creatinine Enzymatic Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000091_b70f541e2f67f0e04ca4f67e0b2ac449_2619d762ee0adf0f8fc44b2f43a4bdd2. The license holder is M/s. Jeev Diagnostics Pvt. Ltd,, and it is classified as Device Class Class B. The approving authority is Tamil Nadu.

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 Enzymatic Test Kit
UID: MFG/IVD/2020/000091_b70f541e2f67f0e04ca4f67e0b2ac449_2619d762ee0adf0f8fc44b2f43a4bdd2

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

This reagent is intended for in vitro quantitative determination of creatinine in serum, plasma and urine

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