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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_349343ab2db9ace1a9cb1363f3b4009e. 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.

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CDSCO Registered
Class Class D
Revascularization Device
UID: IMP/MD/2018/000118_8e7e0dc6a79258796389636d52125b9b_349343ab2db9ace1a9cb1363f3b4009e

Brand Name

Rebar

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Solitaireโ„ข Platinum Revascularization Device is intended to restore blood flow by removing thrombus from a large intracranial vessel in patients experiencing ischemic stroke within 8 hours of symptom onset. Patients who are ineligible for intravenous tissue plasminogen activator (Rebar) or who fail IV t-PA therapy are candidates for treatment

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