Self-Expanding Peripheral Stent System
- UID
- IMP/MD/2018/000172_4e04bf06413147b00062e5ec2e4ce333_ffb1de109e24ecfc26074c123a203224
- Device class
- Class C
- Brand name
- Everflex Self Expanding Peripheral stent with Entrust delivery system
- Approving authority
- CDSCO
- Product information
- Peripheral The stent is indicated for use in the following types of occlusions or lesions: • Occlusions or lesions at high risk for abrupt closure or threatened closure following percutaneous transluminal angioplasty (Everflex Self Expanding Peripheral stent with Entrust delivery system) • Lesions that appear to be at high risk for restenosis following PTA in the common iliac, external iliac, superficial femoral, proximal popliteal, or subclavian arteries Stenting is intended to improve and maintain the artery luminal diameter. Biliary The stent is indicated as a palliative treatment of malignant neoplasms in the biliary tree.
Self-Expanding Peripheral Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000172_4e04bf06413147b00062e5ec2e4ce333_ffb1de109e24ecfc26074c123a203224. This device is marketed under the brand name Everflex Self Expanding Peripheral stent with Entrust delivery system. The license holder is India Medtronic Private Limited ,Shed No. 3, Block No. 1, Survey No. 389, 400/2A & 2C, Pudur Main Road, Kuthambakkam - 600124, Poonamallee Taluk, Tiruvallur District ,Tiruvallur Tamil Nadu ,600124 ,India, and it is classified as Device Class Class C. The approving authority is CDSCO.
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