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Balloon Catheter - India CDSCO Medical Device Registration

Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000389_8ed9cb6bdc14ce1ac902f2894708b919_2d166a3a65f03c569e9039f3e97f3eb6. This device is marketed under the brand name CREDO Stent. The license holder is N-VASCULAR TECHNOLOGY PRIVATE LIMITED, and it is classified as Device Class Class D. 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 D
Balloon Catheter
UID: IMP/MD/2021/000389_8ed9cb6bdc14ce1ac902f2894708b919_2d166a3a65f03c569e9039f3e97f3eb6

Brand Name

CREDO Stent

Device Class

Class D

Approving Authority

CDSCO

Product Information

The NeuroSpeed PTA balloon catheter is indicated for dilation of a stenosis in the cerebral arteries in order to improve perfusion. The NeuroSpeed PTA balloon catheter is indicated for introduction of the self-expanding Credo stent

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