Microcoil
- UID
- IMP/MD/2018/000449_44d7f25b3b40ff4994eebcd0bae4a40a_9dbb8a8f565cf30f0ca238cbe24be356
- Device class
- Class D
- Brand name
- Revive SE
- License holder
- Johnson & Johnson Private Limited
- Approving authority
- CDSCO
- Product information
- The Orbit Galaxy G2 Microcoil Delivery System is intended for endovascular embolization of intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and is also intended for arterial and venous embolizations in the peripheral vasculature.
Microcoil is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000449_44d7f25b3b40ff4994eebcd0bae4a40a_9dbb8a8f565cf30f0ca238cbe24be356. 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.
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