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_ef90e8c6315a9b9420799213e9fd8fd5. 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.
Brand Name
Rebar
License Holder
India Medtronic Private LimitedDevice Class
Approving Authority
CDSCO
Product Information
Mirage 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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