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Self-expandable peripheral stent system - India CDSCO Medical Device Registration

Self-expandable peripheral stent system is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000110_729ef0e0d428e810ff877fe8180cdeca_736b4076db6ccde55af1544e7c9bb6f9. This device is marketed under the brand name Zephyr , Rejuvant. The license holder is Sahajanand Laser Technology Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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 C
Self-expandable peripheral stent system
UID: MFG/MD/2019/000110_729ef0e0d428e810ff877fe8180cdeca_736b4076db6ccde55af1544e7c9bb6f9

Brand Name

Zephyr , Rejuvant

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

The Self-expandable peripheral stent system is indicated in treatment of patients with symptomatic de novo or restenotic native lesions or occlusion of the superficial femoral artery and/or proximal popliteal artery and for peripheral vascular use following failed percutaneous transluminal angioplasty (Zephyr , Rejuvant). It is also indicated for palliative treatment of biliary strictures produced by malignant neoplasm.

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