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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 MFG/MD/2018/000028_0514fb5b31d824c337d4013c6a3753e5_ce82902edeb5f003c91a77f2569f4a85. This device is marketed under the brand name First Brand. The license holder is Meril Life Sciences Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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: MFG/MD/2018/000028_0514fb5b31d824c337d4013c6a3753e5_ce82902edeb5f003c91a77f2569f4a85

Brand Name

First Brand

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

The MeriFlexTM Hydrophilic Guidewire is designed to direct a catheter to the desired anatomical location during diagnostic or interventional procedures

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