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Contec ECG CMS 600 G

Contec ECG CMS 600 G

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1 Ordered
SKU 01.1.5493.00
Manufacturer Contec
€970.96
In stock

2 pieces on stock

Details

ECG600G six channel ECG can sample and simultaneously print out ECG waveforms by using thermal printing system.

Features: ECG waveform recording and display in auto/manual mode; auto-measurement and auto-diagnosis of ECG wave parameters; "No paper" and electrode malfunction alarm system; several interface language options (Chinese, English, Italian, Turkish); database management.

Comprehensive interface enables inquiry into saved ECG wave parameters, auto-analysis and auto-interpretations of ECG wave parameters and auto-interpretation of results.

Technical specifications

800x480 color LCD screen; displays operational status and ECG waveform. Touchscreen and soft-key keyboard enable easier work. AC filter, baseline filter and EMG filter for ECG signal enable high-quality ECG waveform prints. Simultaneous display of 3/6/12 ECG waveform recordings, printer mode, printer sensitivity, speed and filter provides an easier interpretation of results. Simultaneous display of 12 recordings, digital signal processor. Device working capacity while fully charged: standby mode - 4 hours, continuous work mode - 90 minutes, print up to 150 ECG recordings. Built-in high-capacity data saving system, which can save up to 1000 recordings, enabling physicians a more convenient inquiry into result statistics.

Power supply:
AC: 100V-240V; 50-60 Hz
DC - 7.4V; 3700 mAh
Built-in rechargeable lithium battery.
Paper SKU: 01.4.5754.00

Standard work environment

Operating conditions:

  • a) Ambient temperature: +5°C - +35°C
  • b) Relative humidity: ≤80%
  • c) Power supply: AC: 1OOV- 240V,50/60Hz; DC: 7.4V, 3700 mAh rechargeable lithium battery
  • d) Atmospheric pressure: 86kPa ~ l06kPa


Storage and transportation conditions:

  • a) Ambient temperature: -40°C ~ +55 °C
  • b) Relative humidity: ≤95%
  • c) Atmospheric pressure: 50kPa ~ l06kPa
  • Power supply input: Earth-fault and defibrillation protection
  • Lead: Standard 12 leads
  • Patient leak current: <10µA
  • Input impedance: ≥50 MΩ, -3,0 dB
  • Frequency Response: 0.05 Hz - 150 Hz, +0,4 dB
  • Time constant: >3.2s
  • CMRR (Common-mode rejection ratio): >60dB
  • EMG filter interference: 25Hz/35Hz, +0,4dB, -3,0 dB
  • Recording type: Thermal printing system
  • Recording paper specification: 100mm(W) x 20m(L), high-speed thermal printer
  • Paper speed:
    • Auto-recording: 6,25 mm/s, 12,5 mm/s, 25 mm/s, 50 mm/s, error: ±5%
    • Rhythm recording: 6,25 mm/s, 12,5 mm/s, 25 mm/s, 50 mm/s, error: ±5%
    • Manual recording: 6,25 mm/s, 12,5 mm/s, 25 mm/s, 50 mm/s, error: ±5%Sensitivity options: 5/10/20 mm/mV, error: ±5%. Standard sensitivity: 10 mm/mV ±0,2 mm/mV
  • Auto-recording: Record according to designated recording format and auto-measurement mode, automatic lead-change switch, auto-measurement and auto-analysis
  • Manual recording: Record according to designated recording format, manual lead-change switch
  • 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)
  • Safety class: Class I, type CF applied defibrillation-proof element
  • Enduring polarization voltage: ±500 mV
  • Noise level: <15µVp-p
  • Fuse specifications: 2 pcs f5×20mm AC time lag; T250mA/250V(Power Supply:220V)
  • Dimensions: 315 mm(l)×215 mm(w)×77 mm(h)
  • Net weight: 2.25 kg (5 lbs)

 

Safety Measures- The power supply need to be grounded properly before operation

  • In case of doubt the grounding cable is faulty, make sure to use only the internal (built-in) power supply to run the device
  • Please unplug the power supply cable before changing the fuse
  • This device must be operated by trained and expert medical personnel and maintained by a qualified expert
  • The user must read this user manual before operating this device, strictly following the instructions within
  • Even though the device is designed to fully meet the safety conditions, the user must monitor the device operation and observe the patient's condition
  • Please turn off the device and unplug the supply cable before cleaning and disinfecting the device
  • Please do not use this device in the vicinity of flammable anesthetic gases
  • The device can be used on heart directly. In case the device is simultaneously used with a heart defibrillator or other electric stimulation device, please use precordial Ag/AgCl electrodes and ECG-cables with the defibrillation option. In case defibrillation takes longer than five seconds, single-use precordial electrode must be used instead of a metal one which would burn through patient's skin. It is not recommended to use this device simultaneously with other electric stimulation devices. In case it is necessary, a technical expert must be present and issue instructions.
  • Notes regarding ECG-waveform measurement and analysis:
    • (1) Recorded P and Q-waves ware not always accurate in case of EMG and AC interference. The same applies for ST-segment and T-wave with baseline shift
    • (2) In case of winded or unclear ends of S and T-waves, faulty measurement might occur
    • (3) If case of device not registering the R-wave due to unplugged electrodes or low QRS-wave voltage, measured recordings of heart pulse might be inaccurate
    • (4) In case of low QRS-wave voltage, ECG axis measurement and QRS-wave borderline identification might not always be accurate
    • (5) Occasionally, the device might register frequent premature ventricular contraction complexes as dominant heartbeats
    • (6) A combination of multiple arrhythmia types might cause unreliable measurement due to P-wave identification difficulties in such situations
    • (7) The device has a built-in function for auto-analysis which analyses only the ECG-waves that have been recorded, meaning it doesn't apply to all conditions a patient might be subject of. The analysis results might not be in line with a doctor's diagnosis. Therefore, the conclusive diagnosis for each separate patient depends on a doctor's diagnosis based on analysis results, patient's symptoms and other applicable examinations.
  • In case of using the device simultaneously with a high-frequency surgery device, keep electrodes away from the scalpel to prevent burns and cable burnout caused by high-frequency sparking.
  • In case of using the device simultaneously with a defibrillator, make sure not to touch the patient or bed, as well as taking care an ECG electrode doesn't come in contact with a defibrillator electrode in order to prevent sparking from a burning device or patient.
  • Do not use this device in case of interferences caused by heavy-duty equipment. Moreover, keep it away from interference sources such as headphones or cell phones.
  • When the device or any of its accessories reaches its expiration date, it is necessary to dispose of it in accordance with environment protection guidelines and local legislatives and laws.

 

Device Setup and Storage 

  • Device should be used in a room with all the necessary connections
  • Position the device on a flat surface. Avoid strong vibrations and bumps while moving the device.
  • A functional, grounded electric network is required to use this device; otherwise, the device might cause harm to a patient.
  • In case of doubt the grounding cable is faulty, use the built-in power source.
  • AC frequency and voltage value should be in accordance with safety conditions, ensuring an adequate supply of electrical power.
  • Triplex cables must be set up in the distribution network; otherwise a person handling the device or the patient might be subject to an electrocution hazard.
  • Keep the device away from water and do not use or store it in rooms with high air pressure, humidity or temperature, bad ventilation, containing acid or alkaline gases, chemical drugs or excessive amount of dust.
  • Keep the device away from high-voltage cables, x-ray equipment, ultrasound devices and electric therapy devices.
  • In case of using the device simultaneously with a heart defibrillator or other electric stimulation devices, please use precordial Ag/AgCl electrodes.
  • In case defibrillation takes longer than five seconds, single-use precordial electrode must be used instead of a metal one which would burn through patient's skin.It is not recommended to use this device simultaneously with other electric stimulation devices. In case it is necessary, a technical expert must be present and issue instructions.
  • While the device is running, a doctor must be present, carefully monitoring the patient at all times. Unplug the device or remove the electrode/s in order to ensure patient's safety and well-being.
  • Once you are done with using the device, return all functions to their default positions before turning off the device. Carefully remove the electrodes; do not yank them forcefully. Clean the device and its accessories.
  • Overload, amplifier saturation and electrode unplugging might cause the device to stop running.
  • Regular maintenance must be performed on the device and all its accessories (no more than a year must pass without regularly performing maintenance)
  • Electrocardiograph is a type of measurement device and needs to be regularly tested in accordance with local laws.

 

Main Features

  • High resolution thermal printer (8 dpmm), no setup required. Frequency response up to 150 Hz.
  • Clear and accurate tri-channel ECG-waveform recording with real-time continuous monitoring. Monitoring includes lead indicator, sensitivity, paper speed, filter state etc.
  • Only one press of a button to make an ECG-recording is required in automatic mode, which enhances work efficiency.
  • Touch keypad enables an easier use of the device. TFT-screen shows the rosk status of the device, which makes monitoring easier.
  • Safety class: Class I, Type CF
  • AC and DC power supply available. This device comes with a built-in rechargeable lithium-polymer battery.
  • The device can record up to 150 pieces of ECG waveform and continuously print for 90 minutes in optimal DC conditions.
  • The device can store up to 50 different patient records, and not more than 15 separate patient records without an SD-card.
  • Smooth and elegant device design.
  • Liquid ingress protection classification: IPX0 (No specific protection)
  • Classification by degree of safety in vicinity of flammable anesthetic gas convoluted with air (oxygen and dinitrogen oxide): Not suitable for use.
  • High-quality ECG reading enabled through digital signal processing by AC, DFT and EMG filters.
  • Auto-measurement, auto-analysis and auto-diagnosis of regular ECG parameters reduce the amount of work for doctors and improve work efficiency.
  • Work mode classification: Device is designed for continuous work

 

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Contec ECG CMS 600 G

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