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Preeclampsia Test System - India CDSCO Medical Device Registration

Preeclampsia Test System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000001_058d298d0348c6faf2a231e863f5b3fe_88835393352de973b8dce977c0785fe7. This device is marketed under the brand name Lumella. The license holder is Diabetomics Medical (P) Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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
Preeclampsia Test System
UID: MFG/IVD/2019/000001_058d298d0348c6faf2a231e863f5b3fe_88835393352de973b8dce977c0785fe7

Brand Name

Lumella

Device Class

Class B

Approving Authority

Telangana

Product Information

Rapid test to determine the risk for developing preeclampsia

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