Digital Color Spirometer Handheld Lung Volume Device Mouthpiece PC Software App

Description

SP80B Spirometer
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 nose clip (optional)
One power adapter (optional)
One PC software
Physical characteristic
Dimension: 160 mm (L) × 65 mm (W )× 45 mm (H)
Weight: 190 g
Shipping
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2. Your item will be sent via Air mail within 48 hours after payment is received.
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Terms of Sale
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The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If the item is subject to FDA regulation, We will verify your status as an authorized purchaser of this item before shipping of the item.
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