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Hercules™ Sterile Thoracic Stent-Graft System - India CDSCO Medical Device Registration

Hercules™ Sterile Thoracic Stent-Graft System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000220_735e61a85ced2cd41312718be497895c_cdad81bab4beb6ab94b0ad78f9c95bc5. This device is marketed under the brand name Hercules™. The license holder is MicroPort Scientific India 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.

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CDSCO Registered
Class Class D
Hercules™ Sterile Thoracic Stent-Graft System
UID: IMP/MD/2022/000220_735e61a85ced2cd41312718be497895c_cdad81bab4beb6ab94b0ad78f9c95bc5

Brand Name

Hercules™

Device Class

Class D

Approving Authority

CDSCO

Product Information

The HT-LP is intended for interventional treatment of a variety of aortic aneurysms located confined to the straight segment of the vessel, especially for the endovascular treatment of thoracic aortic aneurysms with distal / proximal aneurysm neck length larger than 15mm.

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