Intraluminal Support Device
- UID
- IMP/MD/2021/000078_ea21d8e78ae044752b24da1104645e60_98451412d99025aca8177c2e54b17b26
- Device class
- Class D
- Brand name
- Flow Re-Direction Endoluminal Device
- License holder
- Faith Biotech Pvt. Ltd.
- Approving authority
- CDSCO
- Product information
- The LVIS EVO Device is intended for use with embolic coils for the treatment of intracranial neurovascular diseases
Intraluminal Support Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000078_ea21d8e78ae044752b24da1104645e60_98451412d99025aca8177c2e54b17b26. 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.