Guidewire Retriever Catheter
- UID
- IMP/MD/2020/000119_64ecc5446be39ccda1281e904ff85ca8_b2337afcdfaf3b895874ef0e472e0adf
- Device class
- Class D
- Brand name
- Spectranetics Laser Sheath
- Approving authority
- CDSCO
- Product information
- The Quick-Cross Capture Guidewire Retriever is intended to be used in conjunction with a steerable guidewire to access discrete regions of the vasculature and for guidewire exchange. The Quick-Cross Capture Guidewire Retriever is not intended for use in the coronary, cerebral or carotid vasculature
Guidewire Retriever Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000119_64ecc5446be39ccda1281e904ff85ca8_b2337afcdfaf3b895874ef0e472e0adf. This device is marketed under the brand name Spectranetics Laser Sheath. The license holder is PHILIPS INDIA LIMITED ,UNIT NOS. N3, N4, N5,N6, C/O. EXPEDITORS INTL. INDIA PVT LTD, AIRPORT CARGO LOGISTICS CENTRE II- ACLC2, NR NEW CUST HOUSE ,New Delhi Delhi ,110037 ,India, 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.