Instructions
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
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
Shipping
* Clearance: we will ship your item(s) to your PayPal confirmed address.Please leave me your clear address,telephone,postal code.
* It is the buyers' responsibility to consider duties, taxes and other extra charges by the government in your respective country.
* All items will be dispatched within 2 bussiness day.
* The item will be declared as lower value for shipping only.We'd like to cooperate with you and declare the value of it as you want us to,so that it is more easier for you to clear the custom.
Return - After service
We offer 60 days return policy. 100% satisfaction is our goal!
1.All items are brand new ,with 1years warranty.
2.If you have a defective item, you want to return or discount. Please contact us within 2 days from you receive the shipment.
3.We will refund the money to you when we get the return items or replace item for you.
4. All return items must be returned with it's original packaging and accessories. Customer is responsible for shipping charges on returned items.
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.
