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LiquiBand XL - Wound closure set, topical

Access comprehensive regulatory information for LiquiBand XL - Wound closure set, topical in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Medtronic Australasia Pty Ltd, manufactured by Advanced Medical Solutions Limited in United Kingdom. The device registration started on February 11, 2022.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.

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TGA ARTG Official Data
Class IIa
Class IIa
LiquiBand XL - Wound closure set, topical
Australia TGA ARTG Registered Device
Good Name: Medtronic Australasia Pty Ltd - LiquiBand XL - Wound closure set, topical
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Intended Purpose

Intended for topical application only to hold closed easily approximated skin edges of wounds from surgical incisions, including punctures from minimally invasive surgery, and simple thoroughly cleansed, trauma-induced lacerations. Should be used in conjunction with, but not in place of, deep dermal stitches.

Device Classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration Information
Start Date
February 11, 2022
Effective Date
February 11, 2022
Manufacturer
Country
United Kingdom
Address
Western Wood Way Langage Science Park, Plymouth, Devon, PL7 5BG