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AMMONIA test kit - India CDSCO Medical Device Registration

AMMONIA test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000062_b490a1be418c0d3bf6a85d24adba45a3_f84afc513a06502a74875e95adbeb0de. 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
AMMONIA test kit
UID: MFG/IVD/2020/000062_b490a1be418c0d3bf6a85d24adba45a3_f84afc513a06502a74875e95adbeb0de

Brand Name

Lateral flow Immunochromatographic Method

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

Ammonia (Lateral flow Immunochromatographic Method) reagent kit used for the quantitative determination of ammonia in plasma. This product is used for in vitro diagnosis by professionals

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