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Reperfusion Catheter - India CDSCO Medical Device Registration

Reperfusion Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000227_834fe13571ebe8eb3daca8f6844f5952_a09f16d326791b282fab279f698ed153. This device is marketed under the brand name Neuron MAX 6F Long Sheath. The license holder is M/S ASIA ACTUAL INDIA (OPC) PVT. LTD., 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
Reperfusion Catheter
UID: IMP/MD/2022/000227_834fe13571ebe8eb3daca8f6844f5952_a09f16d326791b282fab279f698ed153

Brand Name

Neuron MAX 6F Long Sheath

Device Class

Class D

Approving Authority

CDSCO

Product Information

As part of the Penumbra System, the Reperfusion Catheters and Separators are indicated for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (Neuron MAX 6F Long Sheath) within 8 hours of symptom onset. Patients who are ineligible for intravenous tissue plasminogen activator (Neuron MAX 6F Long Sheath) or who fail IV t-PA therapy are candidates for treatment

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