Pure Global

Aortic Root Cannula - India CDSCO Medical Device Registration

Aortic Root Cannula is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000202_8803bf8f9c6a63ae5444edd3c3f116e4_7876e45fe5874610ae3fb2948b816739. This device is marketed under the brand name Ezee Oscan. The license holder is KOSDRUG PVT. LTD, and it is classified as Device Class Class D. The approving authority is Sub Zonal Baddi.

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
Powered by Pure Global AI
CDSCO Registered
Class Class D
Aortic Root Cannula
UID: MFG/MD/2020/000202_8803bf8f9c6a63ae5444edd3c3f116e4_7876e45fe5874610ae3fb2948b816739

Brand Name

Ezee Oscan

License Holder

KOSDRUG PVT. LTD

Device Class

Class D

Approving Authority

Sub Zonal Baddi

Product Information

Cannulation technique for left-sided coronary artery surgery

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing