AEROBIKA
Clear airways. Drug-free.
As the patient exhales through the AEROBIKA device, an intermittent valve creates positive pressure pulses that help hold airways open and vibrations that help loosen mucus, moving it towards the upper airways to be cleared with a huff cough. Five resistance settings match the device to each patient's expiratory capacity. It works in any orientation, can be combined with a small-volume nebuliser through a 22 mm port, and disassembles into four parts for cleaning, dishwashing or disinfection.
Key specifications
Why the AEROBIKA OPEP device
Pressure and vibration together
Intermittent resistance creates positive pressure pulses during exhalation that help open weak or collapsed airways, while airway vibrations help thin and loosen mucus.
Five settings, one device
A sliding indicator sets five resistance levels. Clinicians start in the middle and adjust so the patient can exhale comfortably for up to 10 minutes.
Works with nebulised therapy
A 22 mm port lets a small-volume nebuliser deliver bronchodilators or hypertonic saline during OPEP sessions, when advised by a healthcare professional.
Backed by published studies
Trudell cites a real-world study in which 18.5% of AEROBIKA users versus 25.7% of controls had a moderate-to-severe COPD exacerbation within 30 days.
Where it is used
Respiratory clinics, pulmonary rehabilitation, cystic fibrosis and bronchiectasis services, post-discharge COPD care and daily home airway clearance.
In the box
One AEROBIKA OPEP device (four-part assembly) with instructions for use. A version with manometer is available for hospital use. Pack sizes and configurations are confirmed with the quotation.
Clearance & compliance
FDA 510(k) cleared (K123400, AEROBIKA PEP device; K150173, AEROBIKA OPEP device with manometer; product code BWF, 21 CFR 868.5690). Supplied subject to registration in each destination country (MOHAP, DoH, DHA, SFDA or the equivalent authority). Certificates, declarations of conformity, IFUs and registration documents are provided with every quotation. Specifications are indicative and subject to manufacturer change.
Where a country has an official agent or authorised distributor, we source the item through it — or directly from the manufacturer if necessary. Product names, trademarks and images belong to their respective owners.
Questions
Is the AEROBIKA OPEP device available in the UAE and the GCC?
KGG sources the AEROBIKA OPEP device on request for hospitals, respiratory clinics and pharmacies in the UAE, Saudi Arabia, Qatar, Kuwait, Bahrain and Oman, supplied subject to registration in each destination country. Availability is confirmed with each quotation.
How do I get a price?
Add the AEROBIKA device to your quote list or use Request a quote, noting whether you need the standard or manometer version. We reply with pricing, lead time and documents for your country.
Who should not use it?
Trudell lists contraindications including inability to tolerate increased work of breathing, intracranial pressure above 20 mmHg, haemodynamic instability, recent facial, oral or skull surgery, acute sinusitis, epistaxis, oesophageal surgery, nausea, active haemoptysis, untreated pneumothorax and middle-ear pathology.
How often should it be replaced?
After 12 months of use, or immediately if damaged.
Can it be cleaned in a dishwasher?
Yes. The four parts can be washed on the top rack in a basket with a normal cycle and rinse aid. Boiling, steam and chemical disinfection methods are also described in the IFU.
How does it cope with Gulf heat in storage?
Trudell gives a storage range of −40 to +60 °C and a use range of +15 to +40 °C. Store it dry in a clean bag or container.
Request a quote
Get pricing for the AEROBIKA OPEP device.
Tell us the quantity, delivery city and whether you are ordering for a facility, a team or a patient. We reply with pricing, lead time and the regulatory documents for your country.
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