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Post Dilatation Catheter - India CDSCO Medical Device Registration

Post Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000483_b36a9a53901cff7a32a0854da5c52f46_5867059ef0e62aa5bf2777bf1730da9a. This device is marketed under the brand name Serpentile, Serpentile Pro, Serpentile Prime. The license holder is Relisys Medical Devices Limited, and it is classified as Device Class Class C. The approving authority is CDSCO, Zonal office, Hyderabad.

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 C
Post Dilatation Catheter
UID: MFG/MD/2022/000483_b36a9a53901cff7a32a0854da5c52f46_5867059ef0e62aa5bf2777bf1730da9a

Brand Name

Serpentile, Serpentile Pro, Serpentile Prime

Device Class

Class C

Approving Authority

CDSCO, Zonal office, Hyderabad

Product Information

Balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving myocardial perfusion. Balloon dilatation of a coronary artery occlusion, for the purpose of restoring coronary flow in patients with ST-segment elevation myocardial infarction. Balloon dilatation of a stent after implantation.

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