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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/2020/000350_d69bc356951cb011ba7eb177911663b8_b1dc30eeacf17e16e8b5d5fa93b133e5. 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.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class D
Guide Wire
UID: IMP/MD/2020/000350_d69bc356951cb011ba7eb177911663b8_b1dc30eeacf17e16e8b5d5fa93b133e5

Brand Name

HI-TORQUE INFILTRAC Guide Wire , HI-TORQUE INFILTRAC PLUS Guide Wire

Device Class

Class D

Approving Authority

CDSCO

Product Information

The HI-TORQUEโ„ข Guide Wires are indicated to facilitate the placement of the catheter by orienting the catheter tip during percutaneous transluminal coronary angioplasty (HI-TORQUE INFILTRAC Guide Wire , HI-TORQUE INFILTRAC PLUS Guide Wire), percutaneous transluminal angioplasty (HI-TORQUE INFILTRAC Guide Wire , HI-TORQUE INFILTRAC PLUS Guide Wire), and other interventional diagnostic or therapeutic procedures

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