General-purpose catheter connector, sterile; Single use device
- UID
- IMP/MD/2018/000061_4cf3332bba3a71bb8840b3679975ba22_ff0a91278a00c0b5061ecf83f2bbba0e
- Device class
- Class B
- Brand name
- Rubicon 18 Support Catheter
- Approving authority
- CDSCO
- Product information
- The AngioJet Ultra Power Pulse Kit is intended for use only with AngioJet Ultra Thrombectomy Sets indicated for the control and selective infusion of physician specified fluids, including thrombolytic agents, into the peripheral vascular system using the AngioJet Ultra System.
General-purpose catheter connector, sterile; Single use device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000061_4cf3332bba3a71bb8840b3679975ba22_ff0a91278a00c0b5061ecf83f2bbba0e. This device is marketed under the brand name Rubicon 18 Support Catheter. The license holder is Boston Scientific India Private Limited ,C/o Parekh Integrated Services Pvt.Ltd., 1st Floor, Khasra Nos. 9//12/3 min (3-17), 13/3min (5-7), 18(8-0), 19min (5-16), 22min (5-16), 23(8-0), 13//2min (5-16), 3 (8-0), Village Bhangrola, Sector M-12 ,Gurgaon Haryana ,122505 ,India, and it is classified as Device Class Class B. The approving authority is CDSCO.
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