Notification form: Reclassification of active implantable medical devices (AIMD)

Closes 25 May 2022

Opened 8 Dec 2020

Overview

The Therapeutic Goods Legislation Amendment (2019 Measures No.1) Regulations 2019 was made on 12 December 2019 to include the reclassification of active implantable medical devices (AIMD) from Class AIMD to Class III (high risk), effective from 25 November 2021.

From 25 November 2021, active implantable medical devices will be required to be reclassified from Class AIMD to Class III.

What you need to do

If you are a sponsor/manufacturer/distributor of an active implantable medical device and, your device was included in the ARTG prior to 25 November 2021, or you have submitted an application for inclusion in the ARTG for a Class AIMD medical device prior to 25 November 2021 then you need to:

  • Notify the TGA before 25 May 2022 or within 2 months of the start date of your ARTG entry using this form, that you have an inclusion that will need to be reclassified; and
  • Submit an application for your device to be included in the ARTG as a Class III medical device before 1 November 2024.

Transitional arrangements are in place to ensure you can continue to supply your device while you apply for it to be included in the ARTG. To access these arrangements you must submit this form before 25 May 2022. Once you have submitted this form, you will have until 1 November 2024 to submit an application for inclusion in the ARTG. For more information see the guidance document. 

Note

Applications for ARTG inclusion must be accompanied by appropriate conformity assessment documentation. Please ensure you allow sufficient time to obtain your conformity assessment documentation in order to submit your documents with your application.

About this form

Please fill in the details of the active implantable medical devices (AIMD) that will require reclassification. You can complete details for multiple ARTG entries in this one form if each ARTG entry has the same manufacturer and sponsor names. Please complete one ‘page’ for each ARTG entry that requires reclassification. Once you have completed a page (ARTG 1), click the 'Continue' button at the bottom of the page. Doing so will return you to the page titled 'Consultation Contents' where you can select another ARTG page (ARTG 2), if necessary, to fill in similar details for another ARTG entry.

Please note: This form is being hosted on a consultation platform, however it is not a consultation and none of the information that you provide using the form will be published.

Audiences

  • Businesses

Interests

  • Hospitals
  • Regulatory policy
  • Strategic Policy
  • Policy Development