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Dry Powder Inhaler

Dry Powder Inhaler — illustrative device image
PRODUCT OVERVIEW

What this page shows

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.

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.

HANDLING OVERVIEW

How to use

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.

  1. Prepare the capsule

    The published specification identifies size 3 capsule loading. Obtain the device-specific instructions for loading and preparation.

  2. Inhale as instructed

    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.

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Catalog configuration references

These values reproduce the source catalog. Confirm the current specification and exact configuration before a purchasing or engineering decision.

Catalog configuration data
SpecificationPublished value
Actuation MethodPatient Active Inhalation Actuation
Drug FormMicronized DryPowder (Blended With Carriers Such as Lactose)
Dose PreparationRequires Size 3 Capsule Loading
Inspiratory Flow RequirementRequires 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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