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Angiographic Guide Wire - India CDSCO Medical Device Registration

Angiographic Guide Wire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000042_5dd2379e7b35f1a77f8bb5b84b084c26_fa980fc1e3ddc326d4b09df103a453d0. This device is marketed under the brand name Explorer. The license holder is Dolphin Lifescience India LLP, 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
Angiographic Guide Wire
UID: MFG/MD/2019/000042_5dd2379e7b35f1a77f8bb5b84b084c26_fa980fc1e3ddc326d4b09df103a453d0

Brand Name

Explorer

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Guide wire is designed for percutaneous vessel entry using Seldinger Technique to facilitate the subsequent introduction of an intravascular device during Invasive Cardiology process. The guide wire is manufactured from stainless steel which could be coated with PTFE silicone or not

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