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BioGlue Surgical Adhesive - Surgical adhesive/sealant, animal-derived

Access comprehensive regulatory information for BioGlue Surgical Adhesive - Surgical adhesive/sealant, animal-derived in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Cryolife Medical (Australia) Company Pty Ltd, manufactured by Artivion Inc in United States of America. The device registration started on December 21, 2023.

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 III
Class III
BioGlue Surgical Adhesive - Surgical adhesive/sealant, animal-derived
Australia TGA ARTG Registered Device
Good Name: Cryolife Medical (Australia) Company Pty Ltd - BioGlue Surgical Adhesive - Surgical adhesive/sealant, animal-derived
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Intended Purpose

BioGlue Surgical Adhesive is indicated for use as an adjunct to standard methods of surgical repair (such as sutures, staples, and/or patches) to adhere, seal, and/or reinforce soft tissue. Indicated soft tissues are cardiac, vascular, pulmonary, and dural.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
December 21, 2023
Effective Date
December 21, 2023
Manufacturer
Country
United States of America
Address
1655 Roberts Boulevard NW, Kennesaw, Georgia, 30144