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_57d4581d17abee85ccc618fbf7d003db. 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_57d4581d17abee85ccc618fbf7d003db

Brand Name

HI-TORQUE VERSATURN™ F Guide Wire

License Holder

Abbott Healthcare Private Limited

Device Class

Class D

Approving Authority

CDSCO

Product Information

Indicated to facilitate the delivery of catheter-based interventional devices during PTCA and PTA. This guide wire may be used with compatible stent devices during therapeutic procedures. The guide wire may be used to reach and cross a target lesion, provide a pathway within the vessel structure, facilitate the substitution of one diagnostic or interventional device for another, and to distinguish the vasculature. This guide wire may also be used to cross or assist in crossing de novo chronic total coronary occlusions (HI-TORQUE VERSATURN™ F Guide Wire)

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