Guide Wire - India CDSCO Medical Device Registration

Guide Wire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000011_d69bc356951cb011ba7eb177911663b8_368a9a9cf2400f58bc865908446cd623. This device is marketed under the brand name HI-TORQUE VERSATURN™ F Guide Wire. The license holder is Abbott Healthcare 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

Guide Wire

UID: IMP/MD/2023/000011_d69bc356951cb011ba7eb177911663b8_368a9a9cf2400f58bc865908446cd623

Brand Name

HI-TORQUE VERSATURN™ F Guide Wire

License Holder

Abbott Healthcare Private Limited

Device Class

Class D

Approving Authority

CDSCO

Product Information

This HI-TORQUE™ Guide Wire is indicated to facilitate the delivery of catheter-based interventional devices during percutaneous transluminal coronary angioplasty (HI-TORQUE VERSATURN™ F Guide Wire) and percutaneous transluminal angioplasty (HI-TORQUE VERSATURN™ F Guide Wire). This guide wire may also be used with compatible stent devices

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