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Large Diameter Balloon Percutaneous Transluminal Angioplasty Dilatation Catheter - India CDSCO Medical Device Registration

Large Diameter Balloon Percutaneous Transluminal Angioplasty Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000140_361c004d4f59fe1a8afa881b567c93f1_3d052635d97d8ba140d458970a0f256d. This device is marketed under the brand name PTA. The license holder is Cardinal Health Medical Products India Pvt Ltd, and it is classified as Device Class Class B. 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 B
Large Diameter Balloon Percutaneous Transluminal Angioplasty Dilatation Catheter
UID: IMP/MD/2022/000140_361c004d4f59fe1a8afa881b567c93f1_3d052635d97d8ba140d458970a0f256d

Brand Name

PTA

Device Class

Class B

Approving Authority

CDSCO

Product Information

The MAXI LDยฎ PTA catheter is intended to dilate stenoses in peripheral arteries.

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