Flow Diverter
- UID
- IMP/MD/2019/000486_47bc40c912a2339e61755d8d17329f17_0d03c4e29aaa80d21a1ab570080ff11a
- Device class
- Class D
- Brand name
- Aperio® Hybrid Thrombectomy Device
- License holder
- Morulaa Health Tech Pvt Ltd
- Approving authority
- CDSCO
- Product information
- The Derivo Embolisation Device is intended for the treatment of intracranial aneurysms which cannot be treated with other endovascular techniques or in which other endovascular or neurosurgical techniques present a higher treatment risk
Flow Diverter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000486_47bc40c912a2339e61755d8d17329f17_0d03c4e29aaa80d21a1ab570080ff11a. This device is marketed under the brand name Aperio® Hybrid Thrombectomy Device. The license holder is Morulaa Health Tech 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.