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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/2022/000632_1b97e721e419e8744f553c875974319f_85f4937746f8e9f9fb6ba03fd30dc787. This device is marketed under the brand name PREFACE 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/2022/000632_1b97e721e419e8744f553c875974319f_85f4937746f8e9f9fb6ba03fd30dc787

Brand Name

PREFACE GUIDING SHEATH

Device Class

Class D

Approving Authority

CDSCO

Product Information

The intended use of the percutaneous PREFACE Braided Guiding Sheath is for the introduction of intravascular electrophysiology catheters into any cardiac chamber.

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