Guidewire
- UID
- IMP/MD/2022/000292_6f79c5dae2a086e749af43b13df8e910_0edde908af3a70adbf50f8627f9276bd
- Device class
- Class B
- Brand name
- Bard Fluoro 4 Silicone Ureteral stent, Bard Fluoro-4 Silicone Ureteral coil stent
- License holder
- Becton Dickinson India Private Limited
- Approving authority
- CDSCO
- Product information
- Bard guidewires are indicated to provide transurethral and/or percutaneous access into the bladder, ureter or renal pelvis.
Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000292_6f79c5dae2a086e749af43b13df8e910_0edde908af3a70adbf50f8627f9276bd. This device is marketed under the brand name Bard Fluoro 4 Silicone Ureteral stent, Bard Fluoro-4 Silicone Ureteral coil stent. The license holder is Becton Dickinson India Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.
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