Pure Global

Balloon catheter for the Tuba Eustachii - India CDSCO Medical Device Registration

Balloon catheter for the Tuba Eustachii is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000060_4da171921461c7035d13479588c5dfb3_971119f813c6f8087d2c58225c7e3b64. This device is marketed under the brand name TubaVent. The license holder is Smith & Nephew Healthcare 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
Balloon catheter for the Tuba Eustachii
UID: IMP/MD/2021/000060_4da171921461c7035d13479588c5dfb3_971119f813c6f8087d2c58225c7e3b64

Brand Name

TubaVent

Device Class

Class B

Approving Authority

CDSCO

Product Information

The catheter is used for balloon dilatation of the Eustachian tube (TubaVent) in the event of an obstructive tube dysfunction.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing