Systolic Pressure(SYS), Diastolic Pressure(DIA), Mean Pressure(MAP), SpO2 and Pulse rate(PR) can be accurately measured. Compact appearance, comprehensive functions, simple and convenient operation, which is applicable for hospitals, community medical treatment and family. ¦Be applicable for adult, pediatric and neonatal for all-round monitoring, easy operation and high cost performance. ¦Be applicable for medicine, surgery, operating room, ICU/CCU, emergency room, obstetrics and gynecology, pediatrics.Built-in rechargeable Li-polymer battery for uninterrupted monitoring. ¦Compact and flexible appearance, easy for carrying and be suitable for indoor and outdoor(in ambulance) monitoring. ¦Display with 2.8'' (320×240) color TFT LCD and red and yellow highlight LED. ¦Visual and audible alarm for Systolic Pressure(SYS), Diastolic Pressure(DIA), Mean Pressure(MAP), SpO2 and Pulse rate(PR), and upper and lower limit of alarm can be set. ¦Unique Flash memory, storage for up to 2000 NIBP data and 30000 SpO2 data.
¦Convenient and quick in inquiring measurement data, review for NIBP trend graph within 24-hour and SpO2 and Pulse rate(PR) trend graph within 20-hour. ¦Auto measurement interval: adjustable from 1 to 90 minutes. ¦Accuracy: Maximum Mean deviation=±5mmHg, Maximum Standard deviation=8mmHg. ¦Overpressure protection: double protection for software and hardware.Upper and lower limit of alarm. Adopt digital SpO2 technology, which has strong anti-interference capability.
Real-time display SpO2, pulse rate, SpO2 Plethysmogram, bar graph, SpO2 and Pulse rate(PR) trend graph. Standard finger-clip probe for adult, binding probe for neonatal is optional. Accuracy: ±2% in stage of 70%-100%, and unspecified in stage of less than 70%. Accuracy: ±2bpm or ±2%, whichever is greater. Measurement Performance in Weak Filling Condition.SpO2 and pulse rate can be shown. Correctly when pulse-filling ratio is 0.4%, SpO2 error is ±4%; the Pulse rate error is ±2bpm or ±2%, whichever is greater. The deviation between the value measured in the condition of man-made light or indoor natural light and that of darkroom is less than ±1%. An extending tube for blood pressure. Dimension for product: 190(L)×162(W)×240(H)mm. Dimension for packaging: 402(L)×228(W)×320(H)mm. Food and Drug Administration and state and local regulatory agencies.
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.(hereinafter referred to as CONTEC) focusing on research, manufacture and distribution of medical instruments, was founded in 1996 as a high-tech company. CONTEC locates in Economic & Technical Development Zone in Qinhuangdao covered an area of 125 acres and building area of over 100000 square meter, which is one of the largest bases for R & D and production of medical devices in China. Contec hopes to cooperate with international companies to supply more innovative design and advanced. We sincerely welcome you to become one of our global partners.
We are looking forward to establishing a successful business relationship with you. This item is in the category "Business & Industrial\Healthcare, Lab & Dental\Medical & Lab Equipment, Devices\Patient Monitors".The seller is "contecmed" and is located in this country: CN. This item can be shipped worldwide.