CDSCO UID IMP/MD/2018/000059_b0d4afb688dc6df2c063b17ec78b9d88_d9ad5cd9d3aa8cab6ac172c31fc2623b

Non-Vascular Guidewire

Boston Scientific India Pvt. Ltd.,·Device Class Class B·India CDSCO·Brand: Interject Contrast Injection Therapy Needle Catheter
Registration details
UID
IMP/MD/2018/000059_b0d4afb688dc6df2c063b17ec78b9d88_d9ad5cd9d3aa8cab6ac172c31fc2623b
Device class
Class B
Brand name
Interject Contrast Injection Therapy Needle Catheter
Approving authority
CDSCO
Product information
The Jagwire Revolution High Performance Guidewire is indicated for use in selective cannulation of the biliary ducts including the common bile duct, pancreatic duct, cystic duct, and right and left hepatic ducts. The endoscopic guidewire is designed to be used during endoscopic pancreatico-biliary procedures for catheter introduction, exchanges of catheters, cannulas, and sphincterotomes, and to aid in the placement of diagnostic and therapeutic devices
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About this record

Non-Vascular Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000059_b0d4afb688dc6df2c063b17ec78b9d88_d9ad5cd9d3aa8cab6ac172c31fc2623b. This device is marketed under the brand name Interject Contrast Injection Therapy Needle Catheter. The license holder is Boston Scientific India Pvt. Ltd.,, and it is classified as Device Class Class B. The approving authority is CDSCO.

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