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Cartridge loaded I-Seed AgX100 I125 implants - Radionuclide source, therapeutic, brachytherapy, manual, permanent implant

Access comprehensive regulatory information for Cartridge loaded I-Seed AgX100 I125 implants - Radionuclide source, therapeutic, brachytherapy, manual, permanent implant in the Australia medical device market through Pure Global AI's free TGA ARTG database. This AIMD is sponsored by RQSolutions Medical Devices Distribution Support, manufactured by Theragenics Corporation in United States of America. The device registration started on February 26, 2016.

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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AIMD
AIMD
Cartridge loaded I-Seed AgX100 I125 implants - Radionuclide source, therapeutic, brachytherapy, manual, permanent implant
Australia TGA ARTG Registered Device
Good Name: RQSolutions Medical Devices Distribution Support - Cartridge loaded I-Seed AgX100 I125 implants - Radionuclide source, therapeutic, brachytherapy, manual, permanent implant
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Intended Purpose

The Medical Device is intended to treat localized,unresectable tumors with low to moderate radiosensitivity. Tumors may be recurrent, or residual following external beam or excision of primary tumor. The device is presented in a cartridge configuration for storing and dispensing the I125 brachytherapy seeds into seed trains of varying lengths and with variable seed to seed spacing as predetermined by the physician

Device Classification
Risk Class
AIMD
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
February 26, 2016
Effective Date
February 26, 2016
Manufacturer
Country
United States of America
Address
5203 Bristol Industrial Way, Buford, GA, 30518