CA10M Capnograph CO2 Tester

Introduction

Capnograph adopts mainstream method to measure the end-tidal carbon dioxide, airway respiration rate and other parameters. It can detect pulmonary ventilation function and reflect the circulation and pulmonary blood flow condition, as well as indirectly reflect the alveolar ventilation, which is applicable for use in pre-hospital emergency transfer, emergency department, ICU, operating room, neonatology, respiratory department and other occasions. The application population is adult, pediatric and neonate patients. The Capnograph connects with patient’ respiratory tract by the airway adapter and breathing tube.

Features

1)End-tidal CO2 measurement function

2)Respiration rate measurement function

3)Over-limit alarm function for End-tidal CO2 and respiration rate

4)Low battery alarm function

Performance

End-tidal CO2 measurement:

1）Measurement range: 0 ~150mmHg

2）Resolution: 1mmHg

3）Accuracy:

0～40 mmHg：±2 mmHg

41～70 mmHg：±5% of readings

71～100 mmHg：±8% of readings

101～150 mmHg：±10% of readings

Respiration rate measurement:

1）Measurement range: 2rpm～150rbpm

2）Resolution: 1rpm

3）Accuracy: ±1rpm

Safety characteristic:

1）Device type: internally powered equipment

2）Degree of protection against electric shock: type BF applied part

3）Degree of protection against ingress of liquid: IPX2

Accessories

User Manual

Adult gas path adapter

Neonate gas path adapter (optional)

Physical Characteristic

Dimension: 55×52×59mm

Weight: 97g (with batteries)

Working environment

Temperature: 5℃~40℃

Relative humidity: 30%~ 75%, no condensation

Atmospheric pressure: 700hPa~1060hPa

Power supply: DC 3V (2 AAA dry batteries)

Input power: ≤1VA

Buy safe Product

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

Please use under the doctor's instruction

Shipping:

1). We will ship within 1 business day after your payement ;ship from China warehouse by China Post 2-4 weeks Arrival

2).We don't add taxes, VAT or other hidden charges. You pay us what you see  on the invoice, i.e. goods subtotal + shipping cost (not include  duties). Please find out as much as you can about your import taxes in  your own country before bidding the item. You need to pay for the import duties in case that occurred for certain goods, or you may kindly give  us some suggestions about that, we promise to do our best to help you!

About Warranty:

We guarantee new equipment other than accessories to be free from defects  in workmanship and materials for a period of twelve months (six months  for spare parts) from the date of shipment under normal use and service. Our company's obligation under this warranty is limited to repairing,  at our company's option, any part which upon our company's examination  proves defective.

Return Policy:

If you receive a defective item which you want to return, please contact  us within 5 days from the day you receive the item. All return items  must be returned with its original packaging and accessories. If we  confirm the damage happened during the shipment, we will bear the  shipping cost for return.

We will refund the money to you when we get the return items. Or replace item for you free of charge.