Hydrophilic Guidewire - India CDSCO Medical Device Registration

Hydrophilic Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000118_e00b42914b45eba6a93fd726bb90d860_edcc45628f29bb950f4502076dcf3672. 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

Hydrophilic Guidewire

UID: IMP/MD/2018/000118_e00b42914b45eba6a93fd726bb90d860_edcc45628f29bb950f4502076dcf3672

Brand Name

Rebar

License Holder

India Medtronic Private Limited

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Avigo Hydrophilic Guidewire is indicated for general intravascular use to aid in the selective placement of catheters in the peripheral and cerebral vasculature during diagnostic and/or therapeutic procedures. The device is not intended for use in the coronary arteries. The guidewire torque device is intended to facilitate guidewire manipulation during interventional procedures. The guidewire introducer is intended to facilitate guidewire insertion into a catheter hub or through a hemostasis valve

Class D

Guidewire

Brand: Rebar

India Medtronic Private Limited

Class D

Class C