Australia flagARTG 430878

Applicator, surgical sealant, dual-channel

ARTG ID: 430878 · Cryolife Medical (Australia) Company Pty Ltd · Artivion Inc · Class IIa · Started December 14, 2023

Good Name: Cryolife Medical (Australia) Company Pty Ltd - Applicator, surgical sealant, dual-channel

Device classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
430878
Start Date
December 14, 2023
Effective Date
December 14, 2023
Sponsor
Manufacturer
Country
United States of America
Address
1655 Roberts Boulevard NW, Kennesaw, Georgia, 30144
Intended purpose

A dual channel device that enables a surgeon to apply with precision a two-component surgical adhesive to a surgical site. Applicator tips are intended to be used only with the prefilled BioGlue Surgical Adhesive (BioGlue) cartridge/syringe(s) - They allow for the proper mixing of the BioGlue implant material.

About this record

Access comprehensive regulatory information for Applicator, surgical sealant, dual-channel in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 430878 and sponsored by Cryolife Medical (Australia) Company Pty Ltd, manufactured by Artivion Inc in United States of America. The device registration started on December 14, 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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