CDSCO UID IMP/MD/2020/000350_ebb40324c43e2be50a3d6805bfc6b1d2_6564585b0e240fe6c5b7d189656160fd

Guide wire

Abbott Healthcare Private Limited·Device Class Class D·India CDSCO·Brand: HI-TORQUE INFILTRAC Guide Wire , HI-TORQUE INFILTRAC PLUS Guide Wire
Registration details
UID
IMP/MD/2020/000350_ebb40324c43e2be50a3d6805bfc6b1d2_6564585b0e240fe6c5b7d189656160fd
Device class
Class D
Brand name
HI-TORQUE INFILTRAC Guide Wire , HI-TORQUE INFILTRAC PLUS Guide Wire
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 INFILTRAC Guide Wire , HI-TORQUE INFILTRAC PLUS Guide Wire) and percutaneous transluminal angioplasty (HI-TORQUE INFILTRAC Guide Wire , HI-TORQUE INFILTRAC PLUS Guide Wire). This guide wire may also be used with compatible stent devices
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About this record

Guide wire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000350_ebb40324c43e2be50a3d6805bfc6b1d2_6564585b0e240fe6c5b7d189656160fd. This device is marketed under the brand name HI-TORQUE INFILTRAC Guide Wire , HI-TORQUE INFILTRAC PLUS 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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