Silicone Ureteral Stent
- UID
- IMP/MD/2018/000016_cbe35302014741149fa81d4cfabda803_aad75319c8877abaa2cb4344c207d88b
- Device class
- Class B
- Brand name
- BARD Nicore Nitinol Guidewire
- License holder
- Bard India Healthcare Pvt. Ltd.
- 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
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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