Pure Global

Pliable-polymer dental regeneration membrane, tacked - ARTG 235233

Access comprehensive regulatory information for Pliable-polymer dental regeneration membrane, tacked in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 235233 and sponsored by Neoss Australia Pty Ltd, manufactured by Neoss AB in Sweden. The device registration started on March 19, 2015.

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.

Free Database
Powered by Pure Global AI
TGA ARTG Official Data
Class IIb
ARTG 235233
Class IIb
Pliable-polymer dental regeneration membrane, tacked
ARTG ID: 235233
Good Name: Neoss Australia Pty Ltd - Pliable-polymer dental regeneration membrane, tacked
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Intended Purpose

Neoss NeoGen membrane is an implantable temporary non-resorbable device (membrane) for use as a spacer creation barrier in the treatment of local defects in the oral cavity in conjunction with tissue regeneration or augmentation. Neoss membranes are intended to be submerged and clinically implanted more than 30 days with an expected duration of implantation of three to nine months or until bone regeneration is complete.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
235233
Start Date
March 19, 2015
Effective Date
March 19, 2015
Manufacturer
Country
Sweden
Address
Arvid Wallgrens Backe 20, Goteborg, 413 46