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/2021/000742_735e61a85ced2cd41312718be497895c_d9daafd7d28ccf39552f93a0cf0f98d3. This device is marketed under the brand name Hercules™. The license holder is PHOENIX MEDICARE.PVT.LTD, and it is classified as Device Class Class D. The approving authority is CDSCO.
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Brand Name
Hercules™
License Holder
PHOENIX MEDICARE.PVT.LTDDevice Class
Approving Authority
CDSCO
Product Information
The Hercules™ Sterile Thoracic Stent-Graft System 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.
