PTA Balloon Catheter - India CDSCO Medical Device Registration

PTA Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000110_b101711203cae2fa44c17ced25f85b10_b8577ddc88828b9ff2774c745e0a5beb. 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

PTA Balloon Catheter

UID: MFG/MD/2019/000110_b101711203cae2fa44c17ced25f85b10_b8577ddc88828b9ff2774c745e0a5beb

Brand Name

Zephyr , Rejuvant

License Holder

Sahajanand Laser Technology Limited

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

The Vector LD PTA balloon Catheter is intended to dilate stenoses in the carotid, iliac, femoral, ilio-femoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. This device is also indicated for stent post-dilatation in the peripheral vasculature

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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

Class B