Medical information notice: This article explains regulatory and device information. It does not provide medical advice or advice about medicinal cannabis treatment. Patients should speak with their prescribing healthcare practitioner.
Elite II device on a clean surface
Regulatory information should be checked against the current official record before it is used in clinical, pharmacy, or launch materials.

What is the ARTG?

The Australian Register of Therapeutic Goods, or ARTG, is the public register for therapeutic goods that can be lawfully supplied in Australia, including many medical devices. An ARTG entry gives users a way to check sponsor details, product category, device class, and stated intended purpose.

For therapeutic cannabis vaporisation devices, ARTG information matters because it distinguishes a registered medical device record from general consumer vaporiser claims. It also gives healthcare professionals, pharmacies, and patients a common reference point.

What does ARTG Entry 526764 say?

The public TGA record lists Mood State Medical Pty Ltd as the sponsor for ARTG Entry 526764. The product category is Medical Devices, the device class is Class IIb, and the product type is a single heated ambulatory nebulizer.

For the Grenco Medical Elite II, the broader global certification list is Australia ARTG Entry 526764 · Class IIb medical device, Health Canada HC MDL 113029, Medsafe NZ WAND registered, and MDSAP · ISO 13485 manufacturing certification.

The public summary describes the intended purpose as use at home, in a hospital, or in a doctor's office for vaporising cannabis flowers and inhaling cannabinoids derived from them, for the appropriate medical indication as prescribed by a physician. It also states use is intended for patients older than 18 years of age.

What ARTG inclusion does not mean

ARTG inclusion should not be read as personal medical advice, a cannabis product approval, or a guarantee that a device is appropriate for every patient. Medicinal cannabis access, prescribing, and patient suitability remain matters for healthcare professionals and relevant regulatory pathways.

The ARTG record also notes that the public summary is not an ARTG certificate document and that readers should verify current accuracy through the TGA.

How to verify the current record

The safest way to confirm the current status is to use the official TGA website rather than relying only on a downloaded copy or third-party summary.

  • Open the official TGA ARTG Entry 526764.
  • Confirm sponsor name, device class, ARTG start date, and intended purpose.
  • Use the site resource library for local copies and supporting documents.

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