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Digital 3 Channel 12 lead ECG/EKG machine +software Electrocardiograph US seller

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Digital 3 Channel 12 lead ECG/EKG machine +software Electrocardiograph US seller

ECG300G 3 Channel ECG MachinePC Software,USB Cable,12 Leads,Thermal Printer,Color screen Introduction ECG300G is an Electrocardiograph which can collect 12-lead ECG signal and print waveform by the thermal printing system. It features in, recording and displaying ECG waveform in AUTO/Manual mode, measuring and diagnosing ECG waveform parameters automatically, prompting for “Lead off” and “Lack of paper”, multi-language interface, AC/DC, selecting any rhythm lead, case database management. Function 1)Sync collection for 12-lead ECG, adopt digital signal processing technology and get high-quality ECG waveform via power frequency filter, baseline filter and EMG filter of ECG signal. 2)Display of 3/6/12-lead ECG, print mode, sensitivity, paper speed and filter state, etc. on one screen, convenient for contrastively diagnosing. 3)Multiply printing modes and formats, including manual, auto 4×3, auto 3×4+1, auto 3×4, auto 2×6+1, auto 2×6, auto 3-2+1, auto 3-2, auto 1×12+1, auto 1×12, rhythm 4, rhythm 3 and rhythm 2, etc. Waveform length printed can be adjusted, and with time print function, which meets different requirements. 4)With the functions of auto-analysis and auto-diagnosis for routine ECG parameters, provide measurement results and auto-diagnosis conclusion for HR, P-R interval, P Duration, QRS Duration, T Duration, Q-T interval, Q-Tc, P Axis, QRS Axis, T Axis, R(V5), S(V1), R(V5)+S(V1), etc. which reduces the doctor’s burden. 5)Built-in memory stores up to 1000 cases, convenient for case review and statistic. 6)Multi-language(Chinese, English, Spanish, Turkish, Polish, Italian, French, German, Portuguese, Kazakstan, Russian, Ukrainian, Serbian and Slovenian) interface and report. Performance Input mode: floating and defibrillation protection Frequency response: 0.05Hz ~ 150Hz(-3dB~+0.4dB) CMRR: >60dB, >100dB(add filter) Time constant:≥ 3.2s Patient leak current: <10µA Calibration voltage: 1mV Sensitivity: 2.5, 5, 10, 20, 40 mm/mV ±5%, standard sensitivity: 10mm/mV±2% Noise level: <15µVp-p Input circuit current: ≤50nA Input impedance: ≥50MΩ Sampling accuracy: 12-bit Safety classification: class I, type CF and defibrillation-proof applied part Recording mode: thermal printing system Auto record: set record according to auto record format and mode, automatically switching leads, measuring and analyzing. Rhythm record: set record according to rhythm record format and mode, automatically measuring and analyzing. Manual record: set record according to record format, manually switching leads. Measurement parameters: HR, P-R interval, P Duration, QRS Duration, T Duration, Q-T interval, Q-Tc, P Axis, QRS Axis, T Axis, R(V5), S(V1), R(V5)+S(V1) Paper size: 80mm(W)×20m(L) Sampling frequency: 1000Hz EMG interference filter: 25Hz/35Hz (-3dB) Power frequency filter: AC 50Hz/60Hz(-20dB) Paper speed: Auto: 25, 50mm/s, ±5% Rhythm: 25, 50mm/s, ±5% Manual: 5, 6.25, 10, 12.5, 25, 50mm/s, ±5% Power supply: AC: 100V~240V(50/60Hz) DC: 7.4V/3500mAh rechargeable lithium battery Fuse specification: two AC time lag fuse(φ5×20mm), T1.6AL250V Waterproof degree: IPX0 Working mode: continuous working Accessories Standard: A lead cable A limb electrode A chest electrode A thermal recording paper A power cord An earth wire A user manual ECG-Sync software+USB cable Physical characteristic Working environment Temperature: 5℃~40℃ Relative humidity: 25%~95%(non-condensing) Atmospheric pressure: 700hPa~1060hPa Transport and storage environment Temperature: -40℃~+55℃ Relative humidity: ≤95% Atmospheric pressure: 500hPa~1060hPa Dimension: 315mm(L) × 215mm(W) × 77mm(H) Weigh: 1.6Kg Buy safe ProductsThe 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.All of our products are CE approved. If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA’s Center for Devices and Radiological Health. 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 Return – After serviceWe offer 14 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. Terms of SaleThere are not extra taxes,VAT or other unmentioned payment.You pay us with goods subtotal + shipping cost (not includeduties). But you need to pay for the import duties in case that occurred for certain goods, or you may kindly give us some suggestions about that, we promise to do our best to help you! International Buyers – Please Note:Import duties,taxes and charges are not included in the item price or shippingcharges.These charges are the buyer’s responsibility.Please check with your country’s customs office to determine what these additional costs will be prior to bidding/buying.”

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