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VentX - India CDSCO Medical Device Registration

VentX is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000357_bcd5d9c5ea17ddbe79b845c3724b3f82_48f79b0c68b3274a535fad65bb601064. This device is marketed under the brand name Skin Port. The license holder is Bausch & Lomb India Pvt. Ltd., and it is classified as Device Class Class B. 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 B
VentX
UID: IMP/MD/2023/000357_bcd5d9c5ea17ddbe79b845c3724b3f82_48f79b0c68b3274a535fad65bb601064

Brand Name

Skin Port

Device Class

Class B

Approving Authority

CDSCO

Product Information

it is intended for the suction or aspiration of fluids and tissue during surgical procedures. The VentX Console is designed to operate with the VASER Amplifier or as a standalone system.

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