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Hydrophilic Guidewire - India CDSCO Medical Device Registration

Hydrophilic Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000472_0514fb5b31d824c337d4013c6a3753e5_6df0d83cb4abfa9850cb363514343a53. This device is marketed under the brand name Ultraskin. The license holder is M/s LepuCare (India) Vascular Solutions Pvt. Ltd.,, 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
Hydrophilic Guidewire
UID: IMP/MD/2020/000472_0514fb5b31d824c337d4013c6a3753e5_6df0d83cb4abfa9850cb363514343a53

Brand Name

Ultraskin

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Ultraskin Hydrophilic Guide Wire is designed to direct a catheter to the desired coronary arteries during diagnostic or interventional procedure

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