Background

The Philips Respironics BiPAP A30 provides advanced bi-level ventilatory support with enhanced AVAPS for the effective treatment of respiratory insufficiencies. Designed for both hospital and home use, this device ensures seamless patient care transitions with intuitive features and data management capabilities. Created for both hospital and home settings, the BiPAP A30 aids in the treatment of conditions such as Obstructive Sleep Apnea Syndrome (OSAS), Chronic Obstructive Pulmonary Disease (COPD), Amyotrophic Lateral Sclerosis (ALS), and other neuromuscular diseases.

The BiPAP A30 integrates advanced technologies like the Auto-TRAK algorithm and AVAPS (Average Volume Assured Pressure Support) to adapt to the patient’s needs. This ensures not only effective ventilation but also improved comfort by maintaining optimal humidity levels and reducing water ingress through its innovative 'Dry Box' technology. Its consistency in design with other Philips Respironics products, such as CPAP and life support ventilators, allows for an easy transition for patients from clinical settings to home-based care. The easy-to-use interface and low-noise operation further enhance the patient experience, making it a preferred choice for care management.

In 2021, the BiPAP A30 along with several other BiPAP, CPAP, and certain ventilators made between 2009 and 2021 were recalled due to potential health risks caused by the foam used to reduce the noise of the machines. The polyester-based polyurethane (PE-PUR) foam began to break down in high humidity or heat causing users to ingest and breathe in particles of the black foam and the chemicals from the foam insulation. There is a potential for serious injury from the foam with necessary medical intervention.

For more information on bi-level ventilators and other Philips products, visit the Philips Official Website.

Product Identification

The device is white in color and square in shape without the 'Dry Box' attached. It does not come in any other color. When the 'Dry Box' is attached, the overall shape of the device is rectangular. It is approximately 4.6 pounds with the power supply attached. The overall dimensions are: 21.6 cm W x 19 cm L x 11.5 cm H. The model number can be found on the front of the device.

Technical Specifications

  • Ventilation modes: CPAP, S, S/T, PC, T
  • Weight: 2.1 Kgs (with power supply)
  • DC power source: 12 VDC, 5.0 A (external battery), 24 VDC, 4.2 A (power supply)
  • Hybrid ventilation: AVAPS (Average Volume Assured Pressure Support)
  • IPAP: 4 - 30 cm H₂O
  • Size: 21.6 cm W x 19 cm L x 11.5 cm H
  • AVAPS rate: 0.5 to 5 cmH2O/min
  • EPAP: 4 - 25 cm H₂O
  • Battery back-up: 11 hours at IPAP 15 / EPAP 4 cm H2O and 12 BPM
  • Inspiratory time: 0.5 - 3 sec.
  • Target tidal volume (when AVAPS enabled): 200 - 1500 ml
  • Breath rate: 0 - 40
  • Rise time: 1 (100 ms) - 6 (600 ms)
  • Polygraph and polysomnography connections: Direct connection to Alice PDx and Alice6 PSGs, AOM to connect to most PSG systems
  • Triggering and cycling: Digital Auto-TRAK algorithm
  • Noise level: < 30 dBA at 10 cmH2O
  • Humidification: System One humidity control and 'Dry Box' technology
  • Alarms: Patient disconnection, Apnea, Low minute ventilation, Low tidal volume with AVAPS only), High respiratory rate
  • Monitoring: Pressure, tidal volume, minute ventilation, respiratory rate, Leak, I/E ratio
  • Data management: EncorePro 2 and DirectView software Compatible with oximetry module, Advanced detection of residual respiratory events (Apnea/Hypopnea Index, Obstructed Airway Apnea, Clear Airway Apnea, Hypopnea, Periodic Breathing, RERA, Large Leak and Snore)
  • Remote control: Compatible with PC Direct

Additional Information

Philips Respironics BiPAP A30 Product Sheet

NhCare Product Information Page

Biomed Supplier

HCE Information Page

FDA Recall Information