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

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 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.