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Guide Extension Catheter - India CDSCO Medical Device Registration

Guide Extension Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000118_879704a29d255297d8ca270f15e001f4_ec7ab9e45d224c65747ab49bacfdf626. This device is marketed under the brand name GENTLE. The license holder is Relisys Medical Devices Limited, and it is classified as Device Class Class B. The approving authority is Telangana.

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
Guide Extension Catheter
UID: MFG/MD/2020/000118_879704a29d255297d8ca270f15e001f4_ec7ab9e45d224c65747ab49bacfdf626

Brand Name

GENTLE

Device Class

Class B

Approving Authority

Telangana

Product Information

The Relisys Guide Extension Catheter is intended to be used in conjunction with guide catheters to access discrete regions of the coronary Use and/or peripheral vasculature, and to facilitate placement of guide wires and other interventional devices

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