Hydrophilic Guidewire
- UID
- IMP/MD/2018/000118_e00b42914b45eba6a93fd726bb90d860_edcc45628f29bb950f4502076dcf3672
- Device class
- Class D
- Brand name
- Rebar
- License holder
- India Medtronic Private Limited
- Approving authority
- CDSCO
- Product information
- The Avigo Hydrophilic Guidewire is indicated for general intravascular use to aid in the selective placement of catheters in the peripheral and cerebral vasculature during diagnostic and/or therapeutic procedures. The device is not intended for use in the coronary arteries. The guidewire torque device is intended to facilitate guidewire manipulation during interventional procedures. The guidewire introducer is intended to facilitate guidewire insertion into a catheter hub or through a hemostasis valve
Hydrophilic Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000118_e00b42914b45eba6a93fd726bb90d860_edcc45628f29bb950f4502076dcf3672. This device is marketed under the brand name Rebar. The license holder is India Medtronic Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.
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.