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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/2018/000118_97732384403d22e9f450af25b669fd5a_9c191d2fe71a7c9ae669dfceddb1600b. This device is marketed under the brand name Rebar. The license holder is India Medtronic Private Limited, and it is classified as Device Class Class D. 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 D
Guidewire
UID: IMP/MD/2018/000118_97732384403d22e9f450af25b669fd5a_9c191d2fe71a7c9ae669dfceddb1600b

Brand Name

Rebar

Device Class

Class D

Approving Authority

CDSCO

Product Information

Silverspeed guidewire is indicated for general intravascular use to aid in the selective placement of catheters in the peripheral, visceral and cerebral vasculature during diagnostic and/or therapeutic procedures

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