Description

Introduction

Capnograph adopts sidestream 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 as well as indirectly reflect the alveolar ventilation standard. Meanwhile, it can also detect the blood oxygen saturation and pulse.

The Capnograph 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. 

Features

1)End-tidal CO2 measurement function

2)Respiration rate measurement function

3)SpO2 measurement function

4)Pulse rate measurement function

5)Over-limit alarm function for EtCO2、Respiration rate,SpO2 and Pulse rate

6)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～120rbpm

2）Resolution: 1rpm

3）Accuracy: ±1rpm

SpO2 measurement:

1)Measurement range: 30～100 %

2)Resolution: 1%

3)Accuracy: 

               70～100 %：2 %

               0 ～ 69 %：undefinition

Pulse rate measurement:

1)Measurement range: 25～250 bpm

2)Resolution: 1bpm

3)Accuracy: ±2 bpm or ±2%,whichever is greater

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: IPX1

Accessories

User Manual

Blood oxygen probe

Sampling pipe


Physical Characteristic

Dimension: 159*72*31 mm

Weight: 270 g



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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.

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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.        
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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.