SpiroSonic FLO

Functional Diagnostics

SpiroSonic FLO

Uscom · SpiroSonic Flo

Article No. AK-FD-560

SpiroSonic FLO is a high-resolution, digital ultrasonic spirometer based on innovative PureFlow technology. It measures lung function precisely and reliably using half-duplex, digital ultrasound flow measurement without moving parts. This design enables easy and thorough disinfection, minimising the risk of nosocomial infections and significantly enhancing patient safety. The absence of moving mechanical components also contributes to the device's durability and reduces maintenance requirements. Seamless integration with the PC-based SpiroReporter software allows comprehensive analysis, archiving, and documentation of spirometry data. Thanks to automatic calibration before each measurement, the time required for external adjustments is eliminated, significantly optimising workflow in the practice. The extremely low flow resistance is particularly advantageous for diagnostics in children, elderly, or weakened patients. SpiroSonic FLO enables modern, evidence-based lung function diagnostics, enhancing and streamlining existing routines. Additionally, the device's compact and lightweight design facilitates easy handling and portability within clinical settings. Device dimensions: 28 ×

Equipment standard by AKLION.

Specifications

Brand
Uscom
Model
SpiroSonic Flo
Product type
Spirometers
Measurement principle
PureFlow digital ultrasound multi-path flow measurement (half-duplex, single-path)
Flow measurement range
± 14 L/s
Maximum volume
± 20 L
Volume measurement accuracy
± 2.5% or 50 ml, whichever is greater
Flow measurement accuracy
± 2.5% or 50 ml/s, whichever is greater
Sampling rate
100 Hz
Expiratory resistance at 14 L/s
< 0.15 kPa/L/s
Connection
USB 2.0 Type A
Flow tube dimensions
Diameter 30 mm, length 165 mm
Device weight
122 g
Protection rating
IP32
Electrical protection class
BF (patient-applied part protection)
Operating temperature
10 – 40 °C
Relative humidity
5 – 95% non-condensing
Conformity
CE marking in accordance with EU Medical Device Directive