Guidewire - India CDSCO Medical Device Registration

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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CDSCO Registered

Class Class B

Guidewire

UID: IMP/MD/2022/000292_6f79c5dae2a086e749af43b13df8e910_0edde908af3a70adbf50f8627f9276bd

Brand Name

Bard Fluoro 4 Silicone Ureteral stent, Bard Fluoro-4 Silicone Ureteral coil stent

License Holder

Becton Dickinson India Private Limited

Device Class

Class B

Approving Authority

CDSCO

Product Information

Bard guidewires are indicated to provide transurethral and/or percutaneous access into the bladder, ureter or renal pelvis.

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