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Guide Extension Catheter - India CDSCO Medical Device Registration

Guide Extension Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000361_879704a29d255297d8ca270f15e001f4_6024c8a4e62d62ef884646ec8d744d6f. This device is marketed under the brand name GUIDEPLUS II. The license holder is NIPRO MEDICAL (INDIA) 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 Extension Catheter
UID: IMP/MD/2018/000361_879704a29d255297d8ca270f15e001f4_6024c8a4e62d62ef884646ec8d744d6f

Brand Name

GUIDEPLUS II

Device Class

Class D

Approving Authority

CDSCO

Product Information

This device is inserted into coronary arteries and used to guide interventional devices, etc. to affected areas in coronary arteries during procedures such as percutaneous transluminal coronary angioplasty. Notably, this product is placed in front of affected areas that are difficult for interventional devices to reach, and then used to support an interventional device,

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