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_a8352009330bd34b6caaa906fb6aaba7. 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.

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/2023/000011_d69bc356951cb011ba7eb177911663b8_a8352009330bd34b6caaa906fb6aaba7

Brand Name

HI-TORQUE VERSATURN™ F Guide Wire

License Holder

Abbott Healthcare Private Limited

Device Class

Class D

Approving Authority

CDSCO

Product Information

HI-TORQUE™ Guide Wires are indicated to facilitate the placement of balloon dilatation catheters during PTCA and PTA

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