Multi-Parameter Patient Monitor model: Gemini

model: Gemini

Standard Configuration:

- ECG, SpO2, NIBP, TEMP, Resp, PR, Li-ion battery



  • Display: 15.6” TFT (Touchscreen), Resolution: 1366 x 768
  • ECG Lead type: 3-lead, 5-lead
  • ECG waveform: 2 channels, 7 channels, 12 channels
  • 10 waveform display,up to 12-lead ECG analysis
  • Aluminum material shell
  • Fanless design allows for quite care environment
  • MEWS (Modified Early Warning Score)
  • Pacemaker detection
  • ST & arrhythmia analysis
  • SpO2 support PVI and PI, low perfusion 0.2%
  • Support BIS module, NMT module
  • Wired/Wireless/4G connection, support HL7 protocol to HIS
  • SpO2 pulse-tone modulation (Pitch Tone)
  • Night mode, standby mode, venipucture mode
  • Graphical & tabular trend review
  • Rechargeable Lithium-ion Battery
  • 48 hours full disclosure wave review for each patient
  • Dimension: 403×320×185mm (L×W×T)
  • Weight: < 10kg under standard configuration
  • LAN: 1 standard RJ45 port
  • WLAN:IEEE 802.11b/g/n
  • USB: 2 USB connectors
  • HDMI: 1 HDMI monitor connnector
  • Output:1 connector for Nurse call,Defib Sync Analog Output

ใบรับแจ้งรายการละเอียด เลขที่ 65-2-2-2-0014152




  • Whether the patient is admitted or not, the system will give a default value to [Patient Cat.] and [Paced], and the user must confirm that the default value is appropriate for the patient being monitored.
  • For patients with pacemakers, [Paced] must be set to [Yes]. Otherwise, the pacing pulse will be treated as normal QRS wave group, and the system is unable to detect the alarm status of [ECG Signal weak].
  • For patients without a pacemaker, [Paced] must be set to [No]. Otherwise, the system is unable to detect the arrhythmias (including PVCs count) related to ventricular premature beats, and fails to perform S'T segment analysis.



  • To avoid damage to the instrument and to ensure patient safety, please use the accessories specified in this Manual.
  • Please install or carry the instrument properly to prevent damage due to falling, collision, strong vibration or other mechanical force.
  • The electromagnetic fields may affect the performance of the instrument, so that using other devices in the vicinity of this instrument must comply with relevant EMC requirements. For example: mobile phone, X-ray or MRI equipment is likely to be a source of interference, since they will transmit high intensity electromagnetic radiation.
  • Before powering on the device, make sure that the power used by the device complies with the supply voltage and frequency requirements on the equipment label or in the Operator's Manual.
  • When the instrument and accessories are about to exceed the useful life, it must be treated in accordance with relevant local laws and regulations or the hospital's rules and regulations.


Contraindication: N/A