Description


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 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 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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1: We accept payment via PayPal.
2: Please pay the money within 5 days after the auction ended.
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Shipping

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

 2.Please make sure the address and tel number are right,both of the information  is very important for delivery,thank you for your kindly cooperation.

 3.After the shipment,we will add the tracking number on both ebay and paypal  website,you can check it and track it by the number.

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 negative 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.