
DJO Global · Model Aircast Cryo Cuff IC
An integrated pneumatic pump within cooler lid provides automated compression and cold therapy. Simplicity of design and ease of operation makes it ideal for post-operative recovery, trauma, athletic training rooms and home use. Intermittent cold and compression help reduce post-operative swelling. Cryo/Cuff IC provides both gravity and motorized system for flexibility of care. Design details such as a whisper quiet motor, an insulated cuff, and quick pad disconnect make the Cryo/Cuff IC flexible, durable, and mobile.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Pump silent or running with no water movement, pad not cooling.
Root cause: Air lock, insufficient ice / water, a kinked hose, a clogged filter, low power, or the unit below the pad.
Symptoms: Flow drops over time, uneven pad temperature.
Root cause: Debris in the inlet filter.
Symptoms: Pad does not fill, or a Cryo/Cuff will not stay pressurised.
Root cause: Air lock, pad above the unit, or a leak in the pad / cuff.
Symptoms: Water around the unit.
Root cause: Worn connector or lid seal.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Circulation pump | Periodic replacement | $$ | Moderate |
| Inlet filter | Frequent wear item | $ | Easy |
| Therapy pad / cuff | Frequent wear item | $$ | Easy |
| Hose / connector seals | Periodic replacement | $ | Easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
No documents available for this device yet.
Synced live from the FDA openFDA API.
The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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