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Drug Eluting Balloon Catheters - India CDSCO Medical Device Registration

Drug Eluting Balloon Catheters is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000245_73a3012a70feb0696c8ca0432c5db70a_13458b1e2b8e654b40f71b5f88a7c038. This device is marketed under the brand name AcoArt Tulip. The license holder is Mn Solutions, 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
Drug Eluting Balloon Catheters
UID: IMP/MD/2020/000245_73a3012a70feb0696c8ca0432c5db70a_13458b1e2b8e654b40f71b5f88a7c038

Brand Name

AcoArt Tulip

License Holder

Mn Solutions

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Drug eluting balloon (AcoArt Tulip) catheters are indicated for percutaneous transluminal angioplasty (AcoArt Tulip) in patients with obstructive disease of peripheral arteries.

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