TGA Notified Supply
• Authorised Hardware: All products are unfilled, non-medicated Cannabis Vaping Devices imported under Regulation 5A of the Customs (Prohibited Imports) Regulations 1956.
• Compliance Infrastructure: Instavape Australia manages all Essential Principles (EPs), technical notifications, and mandatory 6-monthly volume reporting to the TGA.
• Device Standards: Hardware is supplied based on technical safety and notification status.
The Line in the Sand
• Clinical Autonomy: Our role is strictly limited to the supply of the TGA- Notified products and devices. The determination of patient suitability, the selection of therapeutic substances, and the verification of prescribing authorisations are the exclusive professional responsibility of the dispensing pharmacist.
• Information vs. Advice: We provide technical specifications and notification data to support pharmacy due diligence. We provide no clinical guidance, medical advice, or treatment recommendations.
• Data Isolation: As we do not supply scheduled substances.
• B2B Credentialing: In accordance with the Therapeutic Goods (Vaping Goods—Advertising) Authorisation 2024, access to this product data is restricted to AHPRA-registered professionals and authorised clinical purchasing officers.
• Advertising Compliance: This information is provided for the clinical supply chain and is not for public display or consumer-facing promotion.
• Hardware Sponsorship: Instavape Australia acts solely as the Hardware Sponsor. Liability for clinical outcomes rests entirely with the prescribing and dispensing practitioners.
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Airvape
Arizer
- Arizer Solo 2 User Manual
- Arizer Solo 3 User Manual
- Arizer Air Max User Manual
- Arizer SE User Manual
- Arizer Go (ARGO) User Manual