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Non-Vascular Guidewire - India CDSCO Medical Device Registration

Non-Vascular Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000059_b0d4afb688dc6df2c063b17ec78b9d88_42eb8adaafa2a1a8a932c8dab4e150fc. This device is marketed under the brand name Gold Probe Bipolar Electrohemostasis Catheter. The license holder is Boston Scientific India Private Limited ,C/o Parekh Integrated Services Pvt.Ltd., 1st Floor, Khasra Nos. 9//12/3 min (3-17), 13/3min (5-7), 18(8-0), 19min (5-16), 22min (5-16), 23(8-0), 13//2min (5-16), 3 (8-0), Village Bhangrola, Sector M-12 ,Gurgaon Haryana ,122505 ,India, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered
Class Class B
Non-Vascular Guidewire
UID: IMP/MD/2018/000059_b0d4afb688dc6df2c063b17ec78b9d88_42eb8adaafa2a1a8a932c8dab4e150fc

Brand Name

Gold Probe Bipolar Electrohemostasis Catheter

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Jagwire High Performance Guidewire is indicated for use in selective cannulation of the biliary ducts including, but not limited to the common bile, cystic, right and left hepatic ducts. The Jagwire High Performance Guidewire is designed to be used during endoscopic biliary procedure for catheter introduction and exchanges

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