Intra-vascular Balloon Catheter
- UID
- IMP/MD/2018/000111_c6d90f05cb37b9e16be0e9d035255946_d2eb03cc77c5e522fdb9912fc138280f
- Device class
- Class D
- Brand name
- OptiSite Arterial Perfusion Cannula
- License holder
- Edwards Lifesciences (India) Private Limited,
- Approving authority
- CDSCO
- Product information
- Retrograde Coronary Sinus Cardioplegia Catheters with and without Duraflo treatment are intended for delivery of blood or cardioplegia solution intraoperatively to avoid cardiac damage and aid in myocardial protection. Extracorporeal circuit components with a Duraflo treatment are intended for use in cardiopulmonary bypass when a heparin treated catheter is desired upon initial placement.
Intra-vascular Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000111_c6d90f05cb37b9e16be0e9d035255946_d2eb03cc77c5e522fdb9912fc138280f. This device is marketed under the brand name OptiSite Arterial Perfusion Cannula. The license holder is Edwards Lifesciences (India) Private Limited,, and it is classified as Device Class Class D. The approving authority is CDSCO.
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