Product Description
What this is and who it’s for
- The acapella® DH is a handheld vibratory PEP therapy device used to assist airway clearance for people with mucus retention (examples include COPD, cystic fibrosis, bronchiectasis) and those instructed in PEP therapy. It is intended for single-patient use with a detachable mouthpiece or mask.
Variant identification and how to tell it apart
- Model: acapella® DH (green). The green, translucent body and the product shape identify this as the DH (green) variant of the acapella® family.
- Difference vs adjacent variants: the acapella® DM/blue is the low-flow (blue) variant; the green DH is the higher-flow/higher-resistance variant — choose color/part number to match the patient’s recommended expiratory flow capability.
Specifications and fitness-for-purpose
- Color/variant: green acapella® DH (manufacturer part code 21-1530 for DH with mouthpiece).
- Patient connection: detachable mouthpiece (the device also adapts to masks); device has 22 mm fittings as the family design.
- Intended expiratory flow suitability: DH (green) is recommended for patients able to sustain approximately ≥ 15 L/min expiratory flow for ~3 seconds.
What is included (as shown)
- The listing photo shows the acapella® body with a detachable mouthpiece attached.
- Nothing in the photograph indicates retail box, case pack, or additional accessories (nebulizer adapters, tubing, masks) are included.
Condition and packaging (as shown)
- The photographed unit is not shown in factory-sealed packaging; the mouthpiece is attached and the device is displayed loose. Packaging and sterilization status are unknown.
Usage and care notes
- The acapella® is a mechanical (non-electric) device; frequency and resistance are adjusted via the dial on the body. Clean mouthpiece and body per manufacturer instructions (warm soapy water, rinse, dry) after each use.
Limitations and unsuitability
- Not suitable for patients who cannot generate the recommended expiratory flow for the chosen variant; choose the blue/DM low-flow variant for users who cannot sustain ≥15 L/min for 3 seconds.
- Do not use when contra-indications to PEP therapy are present (recent facial/oral/skull surgery, untreated pneumothorax, active haemoptysis, unstable hemodynamics, etc. — clinical assessment required).
Regulatory, prescription and safety notes
- The acapella® is a medical device; local supplier policies vary on whether a prescription is requested for purchase. Verify local regulatory and supplier prescription requirements before purchase.
Unknowns and buyer caveats
- This listing image does not show retail box or lot/expiry/serial information. Buyers should assume contents and packaging may vary and confirm whether the item is new-in-box or sold loose. See warnings for conflicts and missing information.
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