Balloon Dilatation Catheter
- UID
- IMP/MD/2018/000440_16eb53f14e746dc332d80db12a830d7a_96798a7ccb348631d227125a692b62d8
- Device class
- Class C
- Brand name
- Glidesheath Slender
- License holder
- M/s. Terumo India Pvt. Ltd.
- Approving authority
- CDSCO
- Product information
- It is intended to be used for percutaneous transluminal coronary angioplasty (Glidesheath Slender) for the purpose of improving myocardial blood flow in the localized stenotic lesion of the coronary arteries.
Balloon Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000440_16eb53f14e746dc332d80db12a830d7a_96798a7ccb348631d227125a692b62d8. This device is marketed under the brand name Glidesheath Slender. The license holder is M/s. Terumo India 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.