Angiographic Guide Wire
- UID
- MFG/MD/2019/000042_5dd2379e7b35f1a77f8bb5b84b084c26_fa980fc1e3ddc326d4b09df103a453d0
- Device class
- Class D
- Brand name
- Explorer
- License holder
- Dolphin Lifescience India LLP
- 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
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.