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CREATININE TEST KIT - India CDSCO Medical Device Registration

CREATININE TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000062_8d3c5102faebd18945d7edb68efdb535_c7515d341ef5fea69868ca13b730cef3. This device is marketed under the brand name Lateral flow Immunochromatographic Method. The license holder is Mediclone Biotech Private Limited, 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 TEST KIT
UID: MFG/IVD/2020/000062_8d3c5102faebd18945d7edb68efdb535_c7515d341ef5fea69868ca13b730cef3

Brand Name

Lateral flow Immunochromatographic Method

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

Creatinine Test Kit used for the determination of Creatinine in serum/plasma or in urine based on initial rate method using alkaline picrate. This product is used for in vitro diagnosis by professionals

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