Guide Wire - India CDSCO Medical Device Registration
Guide Wire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000451_d42dbdb38e9d071dcab84df3c925fabd_c0cb460bfb13502986d0a90384152259. This device is marketed under the brand name E-xpand. The license holder is Vibgyor Health Care Pvt. Ltd., and it is classified as Device Class Class B. 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
E-xpand
License Holder
Vibgyor Health Care Pvt. Ltd.Device Class
Approving Authority
CDSCO
Product Information
The JOTEC guide wire facilitates the placement and replacement of catheters in diagnostic and interventional procedures, particularly the treatment of abdominal and thoracic aortic aneurysms involving endovascular prostheses.
Stent Graft System
Brand: BeGraft Peripheral
Stent Graft System
Brand: BeGraft Aortic
Stent Graft Balloon Catheter
Brand: E-xpand
Textile Vascular Graft
Brand: E-vita Thoracic 3G
Textile Vascular Graft
Brand: E-vita Thoracic 3G
Stent Graft System
Brand: E-liac
Stent Graft System
Brand: E-vita Thoracic 3G
Stent Graft System
Brand: E-vita Thoracic 3G
Stent Graft System
Brand: E-vita Thoracic 3G
Stent Graft System
Brand: E-vita Thoracic 3G

