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RESCAN 700 - India CDSCO Medical Device Registration

RESCAN 700 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000320_55b4f3f8c2d0f14618de467bd492274c_0b2cab24c1df08619d752b32c1517b29. This device is marketed under the brand name ZEISS. 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
RESCAN 700
UID: IMP/MD/2023/000320_55b4f3f8c2d0f14618de467bd492274c_0b2cab24c1df08619d752b32c1517b29

Brand Name

ZEISS

Device Class

Class B

Approving Authority

CDSCO

Product Information

The product is intended to intraoperatively acquire high resolution OCT images of anterior and posterior segment of the eye in real time. It enables the application of OCT functionality to an ophthalmic surgical microscope and provides OCT image data to an assistance system. The product includes an interface for remote control by an assistance system

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