Silicone Ureteral Stent - India CDSCO Medical Device Registration

Silicone Ureteral Stent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000016_cbe35302014741149fa81d4cfabda803_aad75319c8877abaa2cb4344c207d88b. This device is marketed under the brand name BARD Nicore Nitinol Guidewire. The license holder is Bard India Healthcare Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

Silicone Ureteral Stent

UID: IMP/MD/2018/000016_cbe35302014741149fa81d4cfabda803_aad75319c8877abaa2cb4344c207d88b

Brand Name

BARD Nicore Nitinol Guidewire

License Holder

Bard India Healthcare Pvt. Ltd.

Device Class

Class B

Approving Authority

CDSCO

Product Information

Indicated to relieve obstruction in a variety of benign, malignant and post-traumatic conditions in the ureter such as stones and / or stone fragments, or other Ureteral obstructions such as those associated with Ureteral stricture, carcinoma of abdominal organs, retroperitoneal fibrosis or Ureteral trauma, or in association with Extracorporeal Shock Wave Lithotripsy (BARD Nicore Nitinol Guidewire). The stent may be placed using endoscopic surgical techniques or percutaneously using standard radiographic technique