Non Compliant Balloon Dilatation Catheter - India CDSCO Medical Device Registration

Non Compliant Balloon Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000042_2b59f6b0e377516dc8e8114e34e6285f_1993751cdc6ecabbf1bd7b070793aaac. This device is marketed under the brand name Explorer. The license holder is Dolphin Lifescience India LLP, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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.

Free Database

CDSCO Registered

Class Class D

Non Compliant Balloon Dilatation Catheter

UID: MFG/MD/2019/000042_2b59f6b0e377516dc8e8114e34e6285f_1993751cdc6ecabbf1bd7b070793aaac

Brand Name

Explorer

License Holder

Dolphin Lifescience India LLP

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Balloon Dilatation Catheter (Explorer) is intended to dilate a stenotic portion of a native coronary artery or a bypass graft stenosis for the purpose of improving myocardial perfusion and also and to be used for post-dilation of stents

Class D

Semi Compliant Balloon Dilatation Catheter

Brand: Explorer

Dolphin Lifescience India LLP

Class D

Class D