Platform features
This propellant-free device uses active inhalation to deliver powder. The manufacturer presents two designs; confirm the selected design and formulation requirements in your enquiry.

A capsule-based, breath-actuated inhaler platform for dry powder formulation projects.
Review the catalog rows below and tell us which container and configuration you need to evaluate.
Illustrative image only. Request a current photograph and specification for the exact configuration.
This propellant-free device uses active inhalation to deliver powder. The manufacturer presents two designs; confirm the selected design and formulation requirements in your enquiry.
This is a brief manufacturer-sourced overview for product evaluation, not a complete Instructions for Use (IFU). Before patient use, obtain the current instructions for the exact device and medicine and follow training from a qualified healthcare professional. Do not choose a dose from the catalog table.
The published specification identifies size 3 capsule loading. Obtain the device-specific instructions for loading and preparation.
The manufacturer describes active inhalation to actuate the device. Follow the supplied instructions and professional training for the breathing technique and completion check.
Source: Manufacturer’s published handling overview, checked 6 September 2026. Preparation, priming quantities, hold times, completion signals and disposal must follow the supplied IFU.
Request the correct instructions ↗These values reproduce the source catalog. Confirm the current specification and exact configuration before a purchasing or engineering decision.
| Specification | Published value |
|---|---|
| Actuation Method | Patient Active Inhalation Actuation |
| Drug Form | Micronized DryPowder (Blended With Carriers Such as Lactose) |
| Dose Preparation | Requires Size 3 Capsule Loading |
| Inspiratory Flow Requirement | Requires Peak Inspiratory Flow Rate> 30L/min |
Source: Wanhai Medical official product page, checked 6 September 2026.
Application names reproduce the source catalog. They do not establish approval or compatibility for a specific drug-device combination.
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