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Aspartate Amino Transferase Test Kit - India CDSCO Medical Device Registration

Aspartate Amino Transferase Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000099_f63c3d61d2d2a5f09642c1d8839791c2_3ff67175ee238a9f9cb00a9db2f09643. This device is marketed under the brand name LDL. The license holder is Matrix Labs 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 Kit
UID: MFG/IVD/2021/000099_f63c3d61d2d2a5f09642c1d8839791c2_3ff67175ee238a9f9cb00a9db2f09643

Brand Name

LDL

License Holder

Matrix Labs Pvt Ltd

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

Aspartate Amino Transferase (LDL) Test Reagent Kit is for the quantitative determination of AST/SGOT in human serum or plasma. The test kit is intended for professional use only

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