CDSCO UID IMP/MD/2020/000220_65a0f6d0b5c62baf6570d931285a336b_7c4536ebf07fcaa7f5561b5c39593ea0

Hernia Mesh Fixation Devices

Morulaa Health Tech Pvt Ltd·Device Class Class C·India CDSCO·Brand: LiquiBand® Exceed™ and LiquiBand® Exceed™ XS
Registration details
UID
IMP/MD/2020/000220_65a0f6d0b5c62baf6570d931285a336b_7c4536ebf07fcaa7f5561b5c39593ea0
Device class
Class C
Brand name
LiquiBand® Exceed™ and LiquiBand® Exceed™ XS
Approving authority
CDSCO
Product information
Intended for use in the surgical procedure; repair of hernias through mesh fixation
Similar products (3)
Other products with the same name or brand
Topical Skin Adhesives
Brand: LiquiBand® Exceed™ and LiquiBand® Exceed™ XS
Morulaa Health Tech Pvt Ltd
Class C
Topical Skin Adhesives
Brand: LiquiBand® Exceed™ and LiquiBand® Exceed™ XS
Morulaa Health Tech Pvt Ltd
Class C
Topical Skin Adhesives
Brand: LiquiBand® Exceed™ and LiquiBand® Exceed™ XS
Morulaa Health Tech Pvt Ltd
Class C
Other products from Morulaa Health Tech Pvt Ltd
Products from the same license holder (10 products)
Electrosurgical Instrument
Brand: Speedboat RS2 8 Fr
Class C
Electrosurgical Instrument
Brand: Speedboat RS2 8 Fr
Class C
Electrosurgical Generator
Brand: Speedboat RS2 8 Fr
Class C
RF-Generator and accessories
Brand: Sutter
Class C
Automated Retinal Disease Assessment (Automated Retinal Disease Assessment )
Brand: ARDA
Class C
Diagnostic Imaging and Processing Software
Brand: CAAS MR Solutions
Class C
Diagnostic Imaging and Processing Software
Brand: CAAS MR Solutions
Class C
Sleep disordered breathing SDB
Class B
Patient interface CPAP/BiPAP face mask
Class B
Earmold custom made
Class B
About this record

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.