Thrombectomy Device
- UID
- IMP/MD/2018/000449_7a75b2c01ef04d31925d7499de13e71b_907c1acb5a1cbd8c707ffbb30a112e4f
- Device class
- Class D
- Brand name
- Revive SE
- License holder
- Johnson & Johnson Private Limited
- Approving authority
- CDSCO
- Product information
- It is intended to restore blood flow in patients with acute ischemic stroke secondary to intracranial occlusive vessel disease by providing temporary bypass across the occlusion and/or by the nonsurgical removal of emboli and thrombi. It may be used with aspiration and with the injection or infusion of contrast media and other fluids
Thrombectomy Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000449_7a75b2c01ef04d31925d7499de13e71b_907c1acb5a1cbd8c707ffbb30a112e4f. This device is marketed under the brand name Revive SE. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.
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.