Pure Global

Revascularization Device - India CDSCO Medical Device Registration

Revascularization Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000118_8e7e0dc6a79258796389636d52125b9b_d8cb1fe5ac44fa5dc3dafb4352ff1c6c. This device is marketed under the brand name Rebar. The license holder is India Medtronic 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class D
Revascularization Device
UID: IMP/MD/2018/000118_8e7e0dc6a79258796389636d52125b9b_d8cb1fe5ac44fa5dc3dafb4352ff1c6c

Brand Name

Rebar

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Solitaireโ„ข X Revascularization Device is designed for use in the flow restoration of patients with ischemic stroke due to large intracranial vessel occlusion. Patients who are ineligible for intravenous tissue plasminogen activator (Rebar) or who fail IV t-PA therapy are candidates for treatment. The Solitaireโ„ข X Revascularization Device should only be used by physicians trained in interventional neuroradiology and treatment of ischemic stroke

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing