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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 MFG/MD/2021/000362_6f79c5dae2a086e749af43b13df8e910_51b00ac291809b2f20856a75f9363a1c. This device is marketed under the brand name Trans Wire-Prime. The license holder is Microtrol Sterilisation Services Pvt Ltd., and it is classified as Device Class Class D. The approving authority is CDSCO -North Zone, Ghaziabad.

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
Guidewire
UID: MFG/MD/2021/000362_6f79c5dae2a086e749af43b13df8e910_51b00ac291809b2f20856a75f9363a1c

Brand Name

Trans Wire-Prime

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Guidewire is a steerable guidewire that are used for the introduction and placement of diagnostic or interventional devices in the coronary and peripheral vasculature and may be used to reach and cross a target lesion. Guidewire are used to facilitate the substitution of one diagnostic or interventional device for another

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