Non-Compliant PTCA Balloon Catheter
- UID
- IMP/MD/2022/000674_ed4fd3ca82a4eadff778a86617f058e1_20eae3d01865da81d72e0b5874ea2a2f
- Device class
- Class D
- Brand name
- BioMatrix NeoFlex
- License holder
- Biosensors Medical India Pvt. Ltd.
- Approving authority
- CDSCO
- Product information
- The Biosensors RISE NC PTCA Balloon Catheter is indicated for: • balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis for the purpose of improving myocardial perfusion • post-delivery expansion of balloon expandable coronary stents
Non-Compliant PTCA Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000674_ed4fd3ca82a4eadff778a86617f058e1_20eae3d01865da81d72e0b5874ea2a2f. This device is marketed under the brand name BioMatrix NeoFlex. The license holder is Biosensors Medical India Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is CDSCO.
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