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UREA BERTHELOT - India CDSCO Medical Device Registration

UREA BERTHELOT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2018/000001_d1f473a86db097d8cd04f2c71f75eaaa_1637f73cda85fe87f2650585c64e4c18. This device is marketed under the brand name LiquiMAX, Lyphomax, Automax and other OEM Brands. The license holder is Avecon Healthcare Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Haryana.

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
UREA BERTHELOT
UID: MFG/IVD/2018/000001_d1f473a86db097d8cd04f2c71f75eaaa_1637f73cda85fe87f2650585c64e4c18

Brand Name

LiquiMAX, Lyphomax, Automax and other OEM Brands

Device Class

Class B

Approving Authority

Haryana

Product Information

Reagent kit for the quantitative kinetic determination of Urea in human serum and plasma

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