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Aspiration Catheter - India CDSCO Medical Device Registration

Aspiration Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000074_2a8968f2cabb23ed5656efad8acdd734_5f79ca256a43d1660aca1f9bd1fee26e. This device is marketed under the brand name 3Flow. The license holder is Biotronik Medical Devices India Pvt Ltd., 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
Aspiration Catheter
UID: IMP/MD/2022/000074_2a8968f2cabb23ed5656efad8acdd734_5f79ca256a43d1660aca1f9bd1fee26e

Brand Name

3Flow

Device Class

Class D

Approving Authority

CDSCO

Product Information

It is intended for use in the central & peripheral circulatory system including saphenous vein grafts, to contain and aspirate embolic material (3Flow) while performing Percutaneous Transluminal Coronary Angioplasty (3Flow) or Percutaneous Transluminal Angioplasty (3Flow) and/or stenting procedures.

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