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Angiography Guidewire - India CDSCO Medical Device Registration

Angiography Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID KTK/28/452/2017_b8bf7ed1a42e4f090ce70b90e9ffb670_54b5b15426ab1f69a62688cbb9bef767. The license holder is RIVARP MEDICAL PVT LTD, and it is classified as Device Class Class D. The approving authority is Sub Zonal Bangalore.

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
Angiography Guidewire
UID: KTK/28/452/2017_b8bf7ed1a42e4f090ce70b90e9ffb670_54b5b15426ab1f69a62688cbb9bef767

Device Class

Class D

Approving Authority

Sub Zonal Bangalore

Product Information

Angiography Guidewire is designed for percutaneous vessel entry using seldinger technique to faciliate the subsequent introduction of an intravascular device during invasive cardiology process. The Guidewire is manufactured from stainless steel which could be coated with PTFE silicone or not

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