Pure Global

Intracranial Support Catheter - India CDSCO Medical Device Registration

Intracranial Support Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000078_a65379609113531f9c6cc0d36b278d27_f7c3d90c11785d131ff1e16089e5e9c8. This device is marketed under the brand name Flow Re-Direction Endoluminal Device. The license holder is Faith Biotech Pvt. Ltd., and it is classified as Device Class Class D. 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 D
Intracranial Support Catheter
UID: IMP/MD/2021/000078_a65379609113531f9c6cc0d36b278d27_f7c3d90c11785d131ff1e16089e5e9c8

Brand Name

Flow Re-Direction Endoluminal Device

Device Class

Class D

Approving Authority

CDSCO

Product Information

The SOFIAยฎ EX Catheter is indicated for general intravascular use, including the neuro and peripheral vasculature. The SOFIAยฎ EX Catheter can be used to facilitate introduction of diagnostic agents or therapeutic devices. The SOFIAยฎ EX Catheter is not intended for use in coronary arteries.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing