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.
Brand Name
Rebar
License Holder
India Medtronic Private LimitedDevice Class
Approving Authority
CDSCO
Product Information
The Solitaireโข 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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Hester Diagnostics Pvt. Ltd., ,Office No. 213/214/214 A/215/216, Jolly Bhavan No. 1, 2nd Floor, 10, New Marine Lines, Taluka Marine Line, District Mumbai Zone1 ,Mumbai City Maharashtra ,400020 ,India
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