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Guiding Sheath - India CDSCO Medical Device Registration

Guiding Sheath is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000497_1b97e721e419e8744f553c875974319f_984bb942efdba02865c879d3580c81dc. This device is marketed under the brand name CARTO VIZIGO BI-DIRECTIONAL GUIDING SHEATH. The license holder is Johnson & Johnson 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
Guiding Sheath
UID: IMP/MD/2022/000497_1b97e721e419e8744f553c875974319f_984bb942efdba02865c879d3580c81dc

Brand Name

CARTO VIZIGO BI-DIRECTIONAL GUIDING SHEATH

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Biosense Webster CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath is indicated for introducing various cardiovascular catheters into the heart, including the left side of the heart through the interatrial septum. The sheath curve can be visualized when used with compatible CARTOโ„ข 3 EP Navigation Systems.

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