Australia TGA ARTG recordIntegra Meshed Dermal Regeneration Template - Dressing, occlusive, collagen
Australia TGA ARTG Registered Device · Integra Neurosciences Pty Ltd · Integra Lifesciences Corporation · Class III · Started December 24, 2021
Good Name: Integra Neurosciences Pty Ltd - Integra Meshed Dermal Regeneration Template - Dressing, occlusive, collagen
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- December 24, 2021
- Effective Date
- December 24, 2021
- Country
- United States of America
- Address
- 1100 Campus Road, Princeton, New Jersey, 08540
It is indicated for the post excisional treatment of full-thickness and partial-thickness injuries where sufficient auto graft is not available at the time of excision or not desirable due to the physiological condition of the patient. INTEGRA Dermal Regeneration Template is also indicated for use in reconstruction of post excisional, full-thickness defects of the integument where there is, in the opinion of the treating surgeon, a potential benefit to the patient by improving the reconstructive outcome or decreasing their mortality/morbidity.
Access comprehensive regulatory information for Integra Meshed Dermal Regeneration Template - Dressing, occlusive, collagen in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Integra Neurosciences Pty Ltd, manufactured by Integra Lifesciences Corporation in United States of America. The device registration started on December 24, 2021.
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.