Description


3.1 Introduction

SPM-D is a device for testing pulmonary function, combining with professional pulmonary function software, it is used to test the patients respiratory function and lung status; it adopts differential pressure collection principle to measure FVC, SVC, MVV, MV and relative parameters, real-time displays respiratory waveform, which is applicable for diagnosis and response evaluation of lung diseases (such as asthma, COPD, pulmonary fibrosis and cough, etc. ), preoperative safety evaluation and routine physical examination, etc. It can be widely used in many scenarios, such as respiratory medicine, thoracic, anesthesiology, surgery, prevention and control institutions of occupational disease, physical examination institutions, etc.

3.2 Features

1) Measure and display over 100 parameters related to FVC, SVC, MVV and MV functions.

2) Display trend chart and respiratory waveform tested, recommend the optimal test curve intelligently.

3) With management functions of user information and case data.

4) Built-in multiple predicted values, which can be set manually.

5) BTPS self-correction function, measure environment parameters automatically.

6) Pulmonary function assessment function.

7) Support bronchial test.

8) With calibration function and quality control, ensure the test accuracy.

9) With quality control function, recommend the test curve with high acceptability intelligently.

10) With report generation, editing and printing functions.

11) One-button test function.

3.3 Performance

Volume range: 0 ~ 10 L

Flow range: 0 L/s ~ 16 L/s

Volume accuracy: ± 3 % or ± 0.05 L (whichever is greater)

Flow accuracy: ± 5 % or ± 0.17 L/s (whichever is greater)

3.4 Accessories

A User Manual

A nose clip

A mouthpiece (disposable)

PC software

3.5 Physical characteristic

Dimension: 143 mm (L) × 84 mm (W) × 41 mm (H)

Weight: 130 g



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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 item 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.

Payment

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Shipping

1. Items are dispatched from China with in 48 hours after payment receiced or eCheck cleared.

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 4. Usually we ship this item from China by air small package,it takes about 10-45 days arrive,and we will supply a tracking number to check its state online.

Terms of Sale



We offer 30 days return policy. 100% satisfaction is our goal!
1. All items are brand new, with 2 years warranty.
2.Client is reaponsible for the custom cleatance and custom duty.
 If any, we will not be responisble for the customs clearance and duty, if you have special requirments for the declaration for your customs office, please contact us before your payment.        
3. Customer is responsible for the returning shipping fee and we will send the replacement after receiving the returned item.
4.  Your positive feedback will be appreciated very much,  and in any case, please do contact us before leaving nagative feedback or ship the item back, we promise we will give you a satisfied answer.

About Us

Contec Medical Systems focusing on research, manufacture and distribution of medical instruments,was founded in 1992
as a high-tech company.
At present there are more than 1200 employees in our company.Our product line covers a wide range of 13 categories.
Most of the domestic hospitals are our customers.
Contec hopes to cooperate with international companies to supply more innovative design and advanced technology products
We sincerely welcome you to become one of our global partners.We are looking forward to establishing a successful business relationship with you.
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