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Rapid Exchange Guide Extension - India CDSCO Medical Device Registration

Rapid Exchange Guide Extension is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000550_6db954218e5ebba8b6d96cc68525aace_6968e588a4bfba6a91101faeedd2cc19. This device is marketed under the brand name Guidion. The license holder is Cardiologix, 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
Rapid Exchange Guide Extension
UID: IMP/MD/2022/000550_6db954218e5ebba8b6d96cc68525aace_6968e588a4bfba6a91101faeedd2cc19

Brand Name

Guidion

License Holder

Cardiologix

Device Class

Class D

Approving Authority

CDSCO

Product Information

Guidion catheters are intended to be used in conjunction with guide catheters to access discrete regions of the coronary and/or peripheral vasculature, and to facilitate placement and exchange of guide wires and other interventional devices

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