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Autorefractor/keratometer - India CDSCO Medical Device Registration

Autorefractor/keratometer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/001181_dfdd1cbf68f0311edbf5463eac65cfc5_96ed2ef44015536d5a41278d800d1428. This device is marketed under the brand name VISUREF. The license holder is Carl Zeiss India (Bangalore) Pvt Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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
Autorefractor/keratometer
UID: IMP/MD/2023/001181_dfdd1cbf68f0311edbf5463eac65cfc5_96ed2ef44015536d5a41278d800d1428

Brand Name

VISUREF

Device Class

Class B

Approving Authority

CDSCO

Product Information

The VISUREF 150 Autorefractor/ Keratometer is a diagnostic instrument used to determine the objective refractive errors and kerato- metric characteristics of the human eye. The results are used to assist the process of prescribing eye glasses and contact lenses.

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