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Hernia Mesh Fixation Devices - India CDSCO Medical Device Registration

Hernia Mesh Fixation Devices is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000220_65a0f6d0b5c62baf6570d931285a336b_7c4536ebf07fcaa7f5561b5c39593ea0. This device is marketed under the brand name LiquiBand® Exceed™ and LiquiBand® Exceed™ XS. The license holder is Morulaa Health Tech Pvt Ltd, and it is classified as Device Class Class C. 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 C
Hernia Mesh Fixation Devices
UID: IMP/MD/2020/000220_65a0f6d0b5c62baf6570d931285a336b_7c4536ebf07fcaa7f5561b5c39593ea0

Brand Name

LiquiBand® Exceed™ and LiquiBand® Exceed™ XS

Device Class

Class C

Approving Authority

CDSCO

Product Information

Intended for use in the surgical procedure; repair of hernias through mesh fixation

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