PTV Dilatation Catheter
- UID
- IMP/MD/2018/000011_216e96578471e527f3f0fc55f3d5e86a_a201a28d315e9d50eed6d96210850b2a
- Device class
- Class C
- Brand name
- Vida® PTV Dilatation Catheter
- License holder
- Bard India Healthcare Pvt. Ltd.
- Approving authority
- CDSCO
- Product information
- The Vida™ PTV Dilatation Catheter is recommended for Percutaneous Transluminal Valvuloplasty of the pulmonary and aortic valves in the following: • A patient with isolated pulmonary or aortic valve stenosis • A patient with valvular pulmonary or aortic stenosis with other minor congenital heart disease that does not require surgical intervention
PTV Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000011_216e96578471e527f3f0fc55f3d5e86a_a201a28d315e9d50eed6d96210850b2a. This device is marketed under the brand name Vida® PTV Dilatation Catheter . The license holder is Bard India Healthcare Pvt. Ltd., and it is classified as Device Class Class C. 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.