Curaleaf International Secures Australian First with TGA Registered Liquid Medical Cannabis Inhalation Device and Extends Availability to New Zealand
Curaleaf International, part of Curaleaf Holdings (TSX: CURA), announced its Que Medical Inhalation Device (QMID) is now available in Australia and New Zealand. The device is the first of its kind approved by Australia's TGA and listed in New Zealand's WAND database. This marks a significant step in expanding access to medical cannabis inhalation devices, addressing a regulatory gap in the Australian market.
How this was made

The 30-second read
Why it matters
Regulatory clearance opens a new revenue stream and strengthens the company's position in the growing medical cannabis market.
Market read
First device of its kind approved in Australia, signaling market expansion for medical cannabis delivery technologies.
What to watch
Device pricing, competition from existing inhalers, and supply‑chain constraints could limit impact.
Background
Curaleaf Holdings (CURA) is a leading U.S. cannabis producer expanding into medical‑device space.
Market effects
Validates medical‑cannabis device pathway, may spur other firms to seek similar approvals.
Adds a regulated inhalation option for Australian and New Zealand patients, potentially boosting local cannabis demand.
Sets precedent for other markets, could influence regulatory approaches worldwide.
Counterpoint
Approval may not translate into significant sales if reimbursement or physician adoption lags.
Key entities
- companyCuraleaf International
Subsidiary of Curaleaf Holdings driving device rollout.
- regulatorTherapeutic Goods Administration (TGA)
Australian authority that approved the QMID device.




