Pure Air 8 Mattress
The Pure Air 8 Mattress is a dynamic, full replacement pressure care system designed for patients at very high risk of pressure injuries. It features true auto-reactive pressure redistribution, continuously adjusting to patient movement and weight to deliver optimal pressure relief and support. The smooth cell alternation cycle minimises shear and discomfort, promoting restful sleep and protecting fragile skin.
- Description
- Features
- Mattress Specifications
- Control Unit Specifications
- Warranties & Standards
- Resources
- Enquiry
- Disclaimer
The Pure Air 8 Mattress is a dynamic, full replacement pressure care system designed for patients at very high risk of pressure injuries. It features true auto-reactive pressure redistribution, continuously adjusting to patient movement and weight to deliver optimal pressure relief and support. The smooth cell alternation cycle minimises shear and discomfort, promoting restful sleep and protecting fragile skin.
Built for safety and ease of use, the mattress offers shock-absorbing support, reinforced edge stability, and an intelligent low-pressure interface to enhance patient positioning and reduce caregiver burden. Its multi-stretch, waterproof, and vapour-permeable cover supports effective moisture management and infection control. With automated functionality, CPR release, transport mode, and audible/visual alarms, the Pure Air 8 provides clinically proven care for acute, palliative, and high-dependency environments.
Features
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Full replacement dynamic system – designed for very high-risk pressure care.
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Auto-reactive pressure redistribution – continuously adapts to patient movement, weight, and positioning.
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Smooth cell alternation cycle – minimises shear forces and enhances patient comfort.
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Shock-absorbing base with reinforced edges – improves postural stability and transfer safety.
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Low interface pressure delivery – ensures gentle, evenly distributed support across high-risk areas.
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Multi-stretch, waterproof, vapour-permeable cover – washable up to 95°C for infection control.
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Safety functions – CPR release, visual/audible alarms, and transport mode.
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Quiet operation – supports rest and reduces agitation.
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Compatible with profiling beds and clinical handling systems.
The Pure Air 8 Mattress is a dynamic, full replacement pressure care system engineered for patients at very high risk of pressure injuries. Designed for acute, long-term, rehabilitation, and palliative care environments, it delivers continuous auto-reactive pressure redistribution, providing clinically effective protection while maintaining patient comfort and safety.
At its core, the Pure Air 8 features a true dynamic alternating pressure system, with integrated sensors that make constant micro-adjustments in response to patient movement, weight, and positioning. This ensures the lowest effective interface pressure is maintained at all times, reducing tissue compression and preventing pressure injury development in immobile or critically ill patients.
The system’s smooth cell changeover cycle minimises shear forces and avoids abrupt pressure shifts, supporting skin integrity and enhancing comfort. This is particularly important for patients with fragile skin, neurological impairment, or sensitivity to sudden movement.
A shock-absorbing base layer and reinforced edge provide additional postural stability and transfer safety. These design features reduce the risk of falls, prevent sliding during repositioning, and support safe mobilisation and rehabilitation, while also easing caregiver handling.
The low-pressure interface technology evenly distributes weight across key anatomical risk areas, including the sacrum, heels, and shoulders. This contributes to pressure ulcer prevention, improved sleep quality, and reduced agitation — all critical outcomes in both high-dependency and end-of-life care.
The mattress is encased in a multi-stretch, waterproof, vapour-permeable cover, which aids moisture management, skin protection, and infection control. The cover is fully removable and machine washable up to 95°C, supporting stringent hygiene standards in both hospital and community settings.
The system is fully automatic, reducing caregiver workload while ensuring therapeutic consistency. Built-in audible and visual alarms, CPR quick-release, and an optional transport mode enhance clinical safety and operational efficiency.
Mattress Specifications
| Feature | Details |
|---|---|
| Product Code | SM032 |
| Max User Weight | 222 kg |
| Dimensions | 200 cm (L) x 90 cm (W) x 20 cm (H) |
| Number of Cells | 20 fully alternating cells |
| Inflated Cell Height | 20 cm |
| Alternation Cycle | 1-in-2 |
| Initial Inflation Time | 30 – 45 minutes |
| Cell Material | TPU (Thermoplastic Polyurethane) |
| Internal Cell Pressure | 20 – 45 mmHg |
| Top Cover | Multi-stretch polyurethane |
| Seams | High-frequency welded |
| CPR Function | Easy-turn dial (deflates within 30 seconds) |
| Transport Mode | 24-hour support via transport cap |
| Cleaning | Machine washable up to 95°C |
Control Unit Specifications
| Feature | Details |
|---|---|
| Dimensions | 28 cm (L) x 11 cm (W) x 20 cm (H) |
| Weight | 2.6 kg |
| Max Inflate | Auto-return to therapy mode after 20 minutes |
| Cell Cycle Time Options | 10 or 15 minutes |
| Pressure Adjustment | Semi-automatic |
| Noise Level | <40 dB(A) |
| Alerts | Audible low-pressure alert with optional mute |
| Control Panel Lock | Yes |
| Risk Category | Very high |
| Warranty | 3 years |
Warranties & Standards
ARTG Number: 363471
Warranty:
| Mattress Internal Components | Three Years |
| Cover | Three Years |
| Pump | Three Years |
| Clinical Service Life – Normal Use | Six Years |
Standards:
| EMDN Code & Term | V080701 Active anti-bedsore medical mattresses |
| Risk Classification | Risk Classification: Class I medical device according to the regulation (EU) 2017/745, Annex VIII, rule 1 |
| Harmonised Standards Applied | EN ISO: 13485:2016, 14971:2012, 15223-1:2016, 10535:2006 |
| Basic UDI-DI | 50564619DYN_PUP3N |
| Quality Management System | ISO-13485-2016 |
| Safety Standards | BS EB 60601-1:2006+A13:2024 IEC 60601-1-11, IEC 60601-1-2, BS EN 61000, IEC 61000-3-3, IEC 61000-3-2, IEC 61000-4-2, IEC 61000-4-4, IEC 61000-4-5, IEC 61000-4-11, IEC 61000-4-8, IEC 61000-4-6, IEC 61000-4-3 |
| Biocompatibility Standards (Skin & Patient Contact) | SO 10993 series — Biological evaluation of medical devices
ISO 10993-1: Evaluation and testing within a risk management process ISO 10993-5: Tests for in vitro cytotoxicity ISO 10993-10: Tests for irritation and skin sensitization ISO 10993-23: Tests for irritation (skin and mucosal surfaces) |
| Infection Control & Hygiene | ISO 16603 / ISO 16604 — Resistance of materials to penetration by blood and body fluids / blood-borne pathogens
EN ISO 22610 — Resistance to wet bacterial penetration (commonly referenced alongside UNI EN 13795) EN ISO 22612 — Resistance to dry microbial penetration ISO 14272 (and related) — Cleanability and disinfectant resistance |
| Flammability Standards (Hospital Safety) | BS 7175 — Flammability testing for bed mattresses and components used in hospitals (UK/NHS standard)
Crib 5 / Source 5 test — Specific ignition resistance test (often cited in Australia & UK healthcare tenders) CAL TB 129 (California Technical Bulletin) — Full-scale flammability test for mattresses EN 597-1 & EN 597-2 — Smouldering cigarette and match flame tests |
| Performance & Durability | SO 12947 (Martindale Test) — Abrasion resistance of fabrics
ISO 811 — Hydrostatic head test (liquid barrier performance) ISO 14126 — Protective clothing against infective agents (often adapted for mattress covers in clinical use) EN 13795 (for surgical textiles, sometimes referenced in infection-barrier bedding) |
Resources
WinnCare product brochures, user guides, certificates and standards, warranties and additional resources and support material available via button link above.
Enquiry
Disclaimer
All product descriptions, indications or advice found on this website are to be used as a guide only, and are by no means a substitute for professional medical advice. Proper use of medical devices requires diagnosis by a physician or physical therapist. Finch Healtchare accepts no responsibility for the improper or uninformed use of it’s products.





