Pure Global

OPHTACATH® - India CDSCO Medical Device Registration

OPHTACATH® is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000414_f206768331bb02af1a266427101efbcd_abf9f0edce479674b56816a36da33c18. This device is marketed under the brand name CONFORMER. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
OPHTACATH®
UID: IMP/MD/2019/000414_f206768331bb02af1a266427101efbcd_abf9f0edce479674b56816a36da33c18

Brand Name

CONFORMER

Device Class

Class B

Approving Authority

CDSCO

Product Information

"The OPHTACATH® balloon catheter is only available in kit. It is used in the treatment of epiphora through the dilatation of an obstructed nasolacrimal duct."

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing