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Guidewire - India CDSCO Medical Device Registration

Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000157_6f79c5dae2a086e749af43b13df8e910_0fa61dab4c9cf0f11e586618e8c7cf7a. The license holder is EURASIA HEALTHCARE LLP, and it is classified as Device Class Class C. 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 C
Guidewire
UID: IMP/MD/2018/000157_6f79c5dae2a086e749af43b13df8e910_0fa61dab4c9cf0f11e586618e8c7cf7a

Device Class

Class C

Approving Authority

CDSCO

Product Information

Guide wire is applicable as an invasive medical device. It is indicated for guiding and assisting insertion of a percutaneous catheter

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