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Vitalograph AIM

Vitalograph AIM

For effective inhaler training on dry powder and metered dose inhalers

The unique Vitalograph AIM™ (Aerosol Inhalation Monitor) is designed to assist medical practitioners in training subjects to use their inhaler correctly. Mastery of the correct technique will support more accurate drug delivery and good patient compliance, resulting in better disease management and fewer visits to medical professionals.

  • Validates effective use of an inhaler
  • Identifies correct choice of inhaler device type
  • Identifies and quantifies poor inhaler technique
  • Objective identification of proper use of the inhaler device
  • Assists in training patients to use their inhalers correctly
  • Provides clear feedback and instructions to subject and trainer
  • Easy to use, hygienic and low cost
  • Can optionally be used with a spacer

I was lecturing and chairing a day on inhaler devices for respiratory physicians. We had a few of the new AIM devices available and these were great in helping us demonstrate correct inhaler device technique; and to provide the doctors with a 'hands-on' opportunity to learn how to do so themselves.

Dr Mark L Levy FRCGP
General Practitioner with Special Interest in Respiratory Disease.

The advantage of the AIM device is that it estimates which part of the lung the drug will be delivered to, dependent upon how the patient inhales; this is therefore a really useful means of training patients to use their inhalers properly, and should be an essential part of a respiratory clinician’s kit in the future if we are to improve compliance and concordance in our patients.

Stephen Foster
Respiratory and Allergy Specialist Pharmacist, Pierremont Healthcare Limited

Vitalograph AIM

Technical Data
Product AIM (Aerosol Inhalation Monitor)
Model Number 4500
Power Supply AAA x 4
Weight Net: 260g (inc batteries and tubing)
Gross: 310g
Dimensions Net: 165mm x 133mm x 39.6mm
Gross: 190mm x 140mm x 65mm
Operating Temperature 10°C - 40°C
Storage Temperature 0°C - 50°C
Storage Relative Humdity 10% - 95%
Safety Standards EN 60601-1:2005
Medical Safety Standard Medical Devices Directive 93/42/EEC1993 as amended
Designed & Manufactured Under ISO 13485:2003, FDA 21CFR820, CMDR & JPAL