Microcoil - India CDSCO Medical Device Registration

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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CDSCO Registered

Class Class D

Microcoil

UID: IMP/MD/2018/000449_44d7f25b3b40ff4994eebcd0bae4a40a_9dbb8a8f565cf30f0ca238cbe24be356

Brand Name

Revive SE

License Holder

Johnson & Johnson Private Limited

Device Class

Class D

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.

Class D

Brand: PROLENE*

Class D