CE Digital Pulmonary Function Lung Volume Device CONTEC SP10 Spirometer+Software

Description

Digital Spirometer sp10
Manufacture:CONTEC Medical Systems
Introduction:
SPIROMETER is a hand-held equipment for checking lung conditions, adopts the infrared mode for measuring relative items, and is applicable for hospital, clinique for routine test.
Features:
Forced Vital Capacity (FVC), Forced Expired Volume in one second (FEV1), the ratio of FEV1 and FVC (FEV1%), Peak expiratory flow (PEF), 25% flow of the FVC (FEF25), 75% flow of the FVC(FEF75) and average flow between 25% and 75% of the FVC(FEF2575) can be measured. Besides, the testee condition can be shown by the ratio of the measured value and the predicted value.
Flow rate-volume chart, volume-time chart display.
Data memory,delete, upload and review.
Trend chart display.
Scaling(Calibration).
Information prompts when volume or flow goes beyond the limits.
Automatic power off when there is no operation in one minute.
Rechargeable lithium battery and with charging tips.
Battery power display.
Performance:
Display mode: 1.8'' color LCD
Display resolution: 160*128
Volume range: 0~10L
Volume accuracy: ±3% or 0.05L (whichever is greater)
Flow range: 1 L/S ~16L/S
Flow accuracy: ±10% or ±0.3L/s(whichever is greater)
Working current: 60 mA
Power supply: DC3.7V rechargeable lithium battery
Safety classification: internally powered equipment, type BF applied part
Accessories:
An User Manual
An USB data line
A mouthpiece
A power adapter
A CD (PC software)
A nose clip(optional)
Physical characteristic:
Dimension: 97mm(L)× 89mm(W)×36mm(H)
Weight: 150g
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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.If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA's Center for Devices and Radiological Health.
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
International Buyer Please note:
★Import duties, taxes and charges are not included in the item price or shipping charge. These charges are buyer's responsibility.
All of our brand machine have 1 year warranty.
★
Return:
If you have a defective item, you want to return,Please contact us within 2 days from you receive the shipment. We will refund the money to you when we get the return items or replace item for you.
All return items must be returned with it's original packaging and accessories. Customer is responsible for shipping charges on returned items.
Only English User manual,Please contact us if you need other language version.