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Aspartate Amino Transferase Test Reagent Kit - India CDSCO Medical Device Registration

Aspartate Amino Transferase Test Reagent Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000091_298f4c10a20ff2196f904c67da1d8301_f9318493678930edf8464f7f6121c3a3. This device is marketed under the brand name identi . 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
Aspartate Amino Transferase Test Reagent Kit
UID: MFG/IVD/2020/000091_298f4c10a20ff2196f904c67da1d8301_f9318493678930edf8464f7f6121c3a3

Brand Name

identi

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

An Aspartate Amino Transferase (identi ) test reagent/kit (identi ) is a medical device intended for the estimation of the enzyme Aspartate Amino Transferase (identi ) in serum / plasma

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