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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/2022/000692_5a35ad56ad19332e653127505267b213_2f0f2141f27b26901e5c95f07883c054. The license holder is Microtrol Sterilisation Services Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Karnataka.

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
GUIDEWIRE
UID: MFG/MD/2022/000692_5a35ad56ad19332e653127505267b213_2f0f2141f27b26901e5c95f07883c054

Device Class

Class B

Approving Authority

Karnataka

Product Information

Guidewire is a device used to facilitate the placement of endourological instruments during diagnostic or treatment procedures. Used for gaining access and navigating tortuous urinary tract

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