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/2018/000016_6f79c5dae2a086e749af43b13df8e910_c8de7eb1cb914b6c0f5fc9ac375bbb44. 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.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered

Class Class B

Guidewire

UID: IMP/MD/2018/000016_6f79c5dae2a086e749af43b13df8e910_c8de7eb1cb914b6c0f5fc9ac375bbb44

Brand Name

BARD Nicore Nitinol Guidewire

License Holder

Bard India Healthcare Pvt. Ltd.

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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