Hot Color LCD hand held spirometer 8 parameters FVC, FEV1, FEV1/FVC,PEF SP80B                                                                                         
    MODEL:SP80B
 
Introduction
The SPIROMETER is a hand-held equipment for checking lung conditions, adopts the infrared signal acquisition mode for measuring items related to FVC, and it is applicable for hospital, clinic, family for routine test.

Functions
Forced Vital Capacity (FVC), forced expiratory volume in one second (FEV1) to forced vital capacity (FVC) ratio (FEV1/FVC), peak expiratory flow (PEF), forced expiratory flow at 25 % of FVC (FEF25), forced expiratory flow at 50 % of FVC (FEF50), forced expiratory flow at 75 % of FVC (FEF75) and forced expiratory flow from 25 %~ 75 % of FVC (FEF2575) can be measured;
The personnel information (including height, age, sex, etc.) can be set.
Flow-volume chart, volume-time chart display.
The data can be stored, deleted, uploaded and reviewed.
Trend chart display.
Health state indication.
Calibration function.
Over - limit prompt function for volume and flow.
Indicate expiration within 6 seconds by indicators.
Start measuring by one-button.
The data can be transmitted by Bluetooth or USB cable.
Real-time clock can be set and displayed.
Battery power indication.
Automatic shutdown when there is no operation within two minutes.

Performance
Display mode: 2.8'' LCD
Volume range: 0 ~ 10 L
Volume accuracy: ± 3 % or ± 0.05 L (whichever is greater)
Flow range: 0 L/s ~16 L/s
Flow accuracy: ± 5 % or ± 0.2 L/s (whichever is greater)
Working current: 200 mA
Power supply: rechargeable lithium battery
Safety class: internally powered equipment, type BF applied part

Accessories
One User Manual
One USB cable
One mouthpiece (disposable accessory)
One PC software

Physical characteristic
Dimension: 160 mm (L) × 65 mm (W )× 45 mm (H)
Weight: 190 g

The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 197923,
and certified by FDA of United States and CE,TUV of Europe. The  Fingertip Pulse Oximeter that is FDA 510K Approved

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