Notification form: Lapses in medical device conformity assessment certification

Closes 22 Jul 2026

ARTG Entry - 20

On this page there are questions related to the twentieth affected ARTG entry. Enter one ARTG entry in the relevant field and provide further information related to this ARTG entry in subsequent fields.

You may add information for up to 20 models included under the affected ARTG entry on this page. If the ARTG entry has more than 20 models, you may submit another form to notify the TGA and list details for all the models across multiple pages. If doing so, please ensure that the ARTG number and name is entered on all pages with model information related to the ARTG entry.

1. ARTG entry - 20
2. Are you intending to cancel the ARTG entry?

If you choose 'Yes' please provide an expected date of cancellation in the field below.

If you choose 'No' or 'Other' please specify in the text box below. You may also add further information related to this ARTG, if required.

By what date will you submit a device cancellation request to the TGA?



3. Do you intend to supply devices included under this ARTG entry after the conformity assessment certification has lapsed?
4. Were all the devices that you are intending to supply manufactured whilst the conformity assessment certification was current and valid?
5. Supply Information

Please provide the requested data per unit of device supplied or expected to be supplied in Australia.

For example, if you supplied 10 units of Model-1 in Australia in the last 12 months (across all UPIs), then enter '10' in the relevant field below. Similarly, if you are expecting to supply 10 units of Model-1 in Australia during the lapsed timeframe (across all UPIs), then enter '10' in the relevant field below. Please note these are number-only fields.