Peripheral support catheter - India CDSCO Medical Device Registration
Peripheral support catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000166_f7d11ccae2d4027eeb3aef4b69949d49_5341215ccf203819b1bb474b25d9cdf2. This device is marketed under the brand name Nitinol. The license holder is M/s Luminor Medical Devices Private Limited, and it is classified as Device Class Class C. 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.
Brand Name
Nitinol
License Holder
M/s Luminor Medical Devices Private LimitedDevice Class
Approving Authority
CDSCO
Product Information
The catheter is intended to facilitate, guide and support a guidewire during access into the peripheral vasculature, allow for guidewire exchanges, and/or provide a conduit for the delivery of saline solutions and/or diagnostic contrast agents. The catheter is indicated for patients with peripheral artery disease in small vessel or challenging anatomy during diagnostic and interventional procedures
Bare Metal Stent – Non-Sterile
Brand: Nitinol
S3V Vascular Technologies Pvt Ltd
Bare Metal Stent – Non-Sterile
Brand: Nitinol
S3V Vascular Technologies Pvt Ltd
Peripheral Balloon Expandable PTFE Covered Stent System
Brand: Nitinol
M/s Luminor Medical Devices Private Limited
Self-expanding peripheral stent system
Brand: Nitinol
M/s Luminor Medical Devices Private Limited