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Alkaline Phosphatase Test Kit - India CDSCO Medical Device Registration

Alkaline Phosphatase Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000099_e5dfdb1a64e5422f56de78e71e7d2d2c_2b5e28f3ed7a666eb7b7d2064234ddf3. 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
Alkaline Phosphatase Test Kit
UID: MFG/IVD/2021/000099_e5dfdb1a64e5422f56de78e71e7d2d2c_2b5e28f3ed7a666eb7b7d2064234ddf3

Brand Name

LDL

License Holder

Matrix Labs Pvt Ltd

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

Alkaline phosphatase (LDL) Test Reagent Kit is for the quantitative determination of alkaline phosphatase in human serum or plasma. The test kit is intended for professional use only

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