19. Periodic Safety Checks 20. Service 21. Disposal of the device after use 22. Declaration of conformity (EU) 23. Emfit warranty, its terms of condition and technical support 24. Technical specifications 25. EMC declaration 26. Declaration of Conformity 27. Disposal of the device after use 28.
It also includes data transfer from the product to • Using the product with a pressure ulcer mattress adjusted with a compressor may disturb functioning the cloud server of Emfit Ltd, which is based on 3G mobile phone technology. Data is available on the of the product.
CAUTION Do not spray, pour or spill liquid onto the power supply, device, cables, or sensor. Product is VCCI certified (in the external power supply). The Emfit device may be surface-cleaned using a soft cloth dampened with either a commercial, nonabrasive cleaner or a Product is UKRSepro certified (in the external power supply).
NOTE! If you choose method B, please notice that you will need an additional computing device during setup: • Mobile device: to create hotspot (Internet connection) • Computing device (laptop, mobile phone or tablet): to set up your Emfit QS device to this hotspot...
NOTE! The electronics unit must be placed on the floor and at minimum 20 cm distance from your body. You can place the EMFIT QS beneath the mattress topper… Minimum of 20 cm distance from body. CLICK!
Fill in the requested password your mattress. This will help prevent sensing (PW: XXX-XXXX-XXX). your partner’s heart rate, especially when you leave the bed earlier than he/she. Emfit Ltd, Finland | Product: Emfit QS | Model: IP-9360 SN: XXXXXX PIN: XXXXX PW: XXX-XXXX-XXX http://192.168.1.3...
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If you cannot access above-mentioned between short pauses. IP-address, check that your computing de- vice did not disable itself from EMFIT QS+- CLINICAL™ and is perhaps again connected to your own Wi-Fi. A problem may especially arise with a desktop computer and a con- nected LAN/ethernet cable.
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If the pairing fails, you will hear three quick tones - low high low - and red light will keep blinking. EMFIT QS device will au- tomatically return to the state it was in at the beginning of this Go to chapter 13.
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12.1.1. MY NETWORK IS HIDDEN If you don’t have the toolbar icon enabled, you can alternatively view it here: First, you will need to find out what type of encryption your home Wi-Fi network uses. With Windows OS computer, move the cursor over the network. WPA2 is a common encryption. Remember this security method’s name as you will use it on next actionstep.
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Next, on the web page in your browser, click “Other network” Type your Wi-Fi network password and click OK. The pass- Red light will stop blinking. Your EMFIT QS device has now button and type your network’s name and choose the correct word you type is visible on purpose because you must en- been configured.
Insert serial number and PIN number of your device. Click “register”. You will be directed to the Emfit QS web appli- cation. YOUR SERIAL NUMBER YOUR PIN NUMBER Click “next”.
15. Meanings of lights and sounds to Access Point (AP) mode How the LED lights and sound notifications of the EMFIT QS+CLINICAL™ behave in different situations. Sound signals are used only during setup to help the user interpret the status of the device.
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Case Red LED light Green LED light Sound EMFIT QS+CARE has an internal memory where sleep data is stored if network or server connection (light on the right) (light on the left) description is lost. Blinking LED lights are used to inform user when device is buffering sleep data to memory and when sleep data is released from memory to Emfit server.
This is caused so called periodic breathing (partial intensifying and to cellular network and Emfit cloud server is established. take more than 10-20 seconds. This is very important: oth- by obstructed upper airways. During hypopneas, upper weakening of breathing).
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The information registered with sleep sensor EMFIT QS+CLINICAL™ can visualize on how different kinds curve represents registered data with different filterings of of breathing disturbances can be detected from data gath- the raw BCG signal. Respiration flow nor saturation cannot ered with the bed sensor.
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2) Periodic obstructive breathing (POB) 3) Prolonged partial obstruction or increased Breating is laboured and the intrathoracic negative respitatory resistance (PPO/IRR) pressure is greater than -8 CmH O. This causes spik- The upper airways of the patient are obstruced ing in he curve in relation to the base line. caused by the increased level of thoracic cavity.
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4) Central apnea Figure 10: Cheyne-Stokes phenomena in the respitatory curve Figure 8: In the left side of the curve, one can see an apnea period when the breathing stops completely. One can also see that there are no attemps to breathe neither. These are features of central sleep apnea. Conclusions 5) Cheyne-Stokes breathing Cheyne-Stokes breathing is a periodic sleep disorder, which has crescendo-diminuendo...
• My sleep period is too long Too long sleep periods are usually caused by the device not reg- • EMFIT QS fails to connect to my wireless network (fail sound istering that you have left the bed. If you need to remove power...
- Inspection of safety labels for legibility. 20. Service The device should only be opened by Emfit service personnel. It contains no user serviceable parts. It does not require routine servicing or calibration. If servicing is necessary, contact Emfit service personnel or your local Emfit representative 21.
Cable length: 3.0 meters Actions in warranty repairs The customer has to contact the vendor or Emfit Ltd and agree upon sending the device to war- Total weight with cable: 278 grams ranty repair. Tell the serial number (found at the back of the electronics device), purchase date, Surface material and color (sensor): defect description and your own contact information.
25. EMC declaration Guidance and manufacturer’s declaration – electromagnetic immunity The product is intended for use in the electromagnetic environment specified below. The customer or the user of the equipment should assure that it is used in such an environment. Immunity test IEC 60601-1-2 Ed.
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150 kHz – 80 MHz equipment should be used no closer to any field strength in the location in which the Emfit Tonic-Clonic Seizure Monitor is used exceeds the applicable RF compliance part of the product, including cables, than the level above, the Emfit Tonic-Clonic Seizure Monitor should be observed to verify normal operation.
26. Declaration of Conformity We, Emfit Ltd, Konttisentie 8, 40800 Vaajakoski, Finland, declare under our sole responsibility that the following product family, EN 60950-1 2006+A2:2013 Information technology equipment - Safety - Part 1: General requirements Product trade name: EMFIT QS+CLINICAL...
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