Home » Products » Lung function » PowerCube Body+
PowerCube Body+
Plethysmographic cabin with flow measurement via ultrasonic sensor.
Body plethysmography is a highly sensitive lung measurement used to detect complex or mixed lung pathologies that might be missed with conventional pulmonary function tests.
- Plethysmographic cabin with ultrasonic flow sensor measurement that does not require calibration.
- Uses a resistance-free measurement sensor, making the procedure more comfortable for the patient.
- Real time exhaled gas determination.
- Real-time ATP–BTPS calculation.
- Resistance-free measurement sensor.
- Calibration measurement programs.
- Advanced diagnostic capability.
- 3D support arm that can be easily adjusted.
- Automatic and simultaneous calibration of both, the cabin and the mouth pressure, at three different frequencies.
- BodyLiveCal to test TGV.
- Standard measurement applications: FVC (including flow-volume loops), pediatric and adult incentive, slow SVC spirometry.
- Complies with ATS/ERS standards.
- Suitable for pediatric, adult, and geriatric patients.
- It uses LFX, an intuitive and easy-to-use software that integrates our pulmonary function tests (spirometry, oscillometry, and body plethysmography) into a single platform.
- Seamless bidirectional connectivity supports a paperless workflow and saves time.
- Its bidirectional communication capability through Ethernet and Wi-Fi enables the fastest automatic transmission to PDF exports or EMR systems, improving workflow.
Hospital, Pediatricians, Pulmonologist, and Research.
* CPT codes and reimbursements are provided as an example only and constitute no promise by SCHILLER or its subsidiaries regarding coverage or payment.
Connect with us today
Contact your SCHILLER representative today if you are interested in learning more or scheduling a demo.
SCHILLER reserves the right to make changes in design, specifications and features shown, or discontinue the product described at any time without notice or obligation. Images may be representative. Device availability in your market is subject to regulatory approval.