Spirometer Lung Breathing Diagnostic Device FVC SVC MVV MV +PC SW CONTEC SPM-D 

               

Instructions

SPM-D is a device for testing pulmonary function, combining with professional pulmonary function software, it is used to test the patient’s 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.


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.


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)


Accessories

A User Manual

A nose clip

A mouthpiece (disposable)

PC software


Physical characteristic

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

Weight: 130 g



Buy safe products

The following FDA Disclaimer is required for all eBay listing in Healthcare category and is included for REFERENCE: 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

International Buyer--Please note:

Import duties,Taxes are not included in the item price.These charges are buyers' responsibility


We are the manufacturer of medical equipment for 17 years, the following are our main products:

ECG /  ECG holter   EEG / EEG Holter      B-ultrasound

Patient Monitor      Fetal doppler             Fetal Monitor 

Spo2 Monitor          Stethoscope              Medical Image....

Agent in the world!

We are look for partners in the world now!

Do you want  to become our agent in you conutry?

Join US!

Skype:xuebox3

contec.med.mary at hotmail.com


               
           
        
        
   

Only English User Manual,Please contact us if you need other language version.thank youibay365