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Coronary Artery Ostial Cannula - India CDSCO Medical Device Registration

Coronary Artery Ostial Cannula is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000100_b00a0e8618de1a79548c03ddd224500f_5f2fb2ae85117e145977c022290df421. This device is marketed under the brand name HSIL. The license holder is HEMANT SURGICAL INDUSTRIES LIMITED, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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
Coronary Artery Ostial Cannula
UID: MFG/MD/2021/000100_b00a0e8618de1a79548c03ddd224500f_5f2fb2ae85117e145977c022290df421

Brand Name

HSIL

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Coronary artery Ostial cannula are intended for use in delivery of cardioplegia solution directly to the coronary arteries during cardiopulmonary bypass surgery

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