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Balloon Dilatation Catheter - India CDSCO Medical Device Registration

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.

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CDSCO Registered
Class Class C
Balloon Dilatation Catheter
UID: IMP/MD/2018/000440_16eb53f14e746dc332d80db12a830d7a_96798a7ccb348631d227125a692b62d8

Brand Name

Glidesheath Slender

Device Class

Class C

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.

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