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_d4d50f690545245b66050dffa55b4485. 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.

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CDSCO Registered

Class Class D

Guidewire

UID: IMP/MD/2018/000118_97732384403d22e9f450af25b669fd5a_d4d50f690545245b66050dffa55b4485

Brand Name

Rebar

License Holder

India Medtronic Private Limited

Device Class

Class D

Approving Authority

CDSCO

Product Information

X-Pedion 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