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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/2023/000586_6f79c5dae2a086e749af43b13df8e910_43367359270ec02445472937dc0bfefe. The license holder is Advanced LifeSciences Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is South Delhi Division.

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/2023/000586_6f79c5dae2a086e749af43b13df8e910_43367359270ec02445472937dc0bfefe

Device Class

Class B

Approving Authority

South Delhi Division

Product Information

ALSPLโ€™s guidewires are intended to facilitate percutaneous vessel entry or placement of devices during diagnostic and interventional procedures, typically using the Seldinger technique. The guidewires are used for urology, gastroenterology or peripheral vascular applications

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