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Summary of Contents for Monitor Monidrop W
- Page 1 MONIDOR ® Monidrop W Infusion monitor Operating manual Software version 1.X.X 0598...
- Page 2 SISÄLTÖ...
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Page 3: Table Of Contents
SISÄLTÖ 1 Monidrop® W infusion monitor / General 1.1 General 1.2 Attaching Monidrop to a drip chamber 1.3.1 Purpose of use 1.3.2 Use 1.3.3 Blood transfusion 1.3.4 Other infusion factors 1.3.5 Safety standards 2 Symbols / Menu structure 3 Using the device 3.1 Activation and start of infusion... -
Page 4: Monidrop® W Infusion Monitor / General
1 GENERAL 1 Monidrop® W infusion monitor / General 1.1 General Drip detector Green light: Infusion in progress Yellow light: Notification Brackets for various drip chambers. Screen Notification button Drip size Latch, indication press to open Power button Charging port is locat- ed at the bottom of the device. -
Page 5: Attaching Monidrop To A Drip Chamber
1 GENERAL 1.2 Attaching Monidrop to a drip chamber 1. Open the locking mechanism by press- ing the locking lever and open the latch. With collar Without collar 2. Put the drip cham- ber into place as shown in the figures. Note the correct po- sitioning of different types of drip chamber... - Page 6 1 GENERAL Correct positions of drip chambers: Figure 2. Drip chamber without Figure 1. Drip chamber with a a collar collar Back Front Back Front Place the drip chamber in the Monidrop® W device so that the air intake cap points forwards or backwards. If the drip chamber has a collar, guide the edge of the collar to the lower slot (Figure 1).
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Page 7: Purpose Of Use
1.3 PATIENT SAFETY 1.3 Patient safety 1.3.1 Purpose of use The Monidrop® W infusion monitor is intended for the periodic or con- tinuous measurement of parenteral fluids via an intravenous route. The Monidrop® W infusion monitor is used for dosage measurements in intravenous therapy. - Page 8 • The device must not be used during magnetic resonance imaging (MRI). • The Monidrop® W infusion monitor is designed as a measuring de- vice for the administration of basic fluids, nutritional solutions, blood products or antibiotics. The device is not applicable for use together with strong medicinal substances requiring high accuracy.
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Page 9: Blood Transfusion
Do not use the device if its charger or cable is damaged. 1.3.3 Blood transfusion • The Monidrop® W infusion monitor can be used to monitor infusion of blood products. Only use disposable products intended and indicated for blood products. The drip size of the blood line must be... -
Page 10: Other Infusion Factors
• If the Monidrop® W infusion monitor is used at temperatures lower than the indicated operating conditions, it must be kept at room temperature for at least one hour before use. -
Page 11: Symbols / Menu Structure
2 SYMBOLS / MENU STRUCTURE 2 Symbols / Menu structure Device symbols: Power switch On/Off Notification button Näytön symbolit: Device or drip chamber tilted Battery status Infusion rate more than 1,200 Mute ml/h Sound on Infusion rate less than 6 ml/h Drip indicator Unstable drip detection Remotely set target limit... - Page 12 2 SYMBOLS / MENU STRUCTURE Label: Symbol Description of symbols Note: Read the instructions delivered with the product. Drip size: 20 drops (gtt)/ml Markings of electrical and electronic equipment in accordance with direc- tive 2002/96/EC (waste electrical and electronic equipment) CE marking in accordance with direc- 0598 tive 93/42/EEC...
- Page 13 2 SYMBOLS / MENU STRUCTURE Main screen (measurement view) The top row indicates the device status; battery status, infusion rate and notification sound. Treatment duration Current infusion rate Liquid volume administered during treatment If the line in the adjacent figure is shown for the current infusion rate, the measurement result is uncertain or the drip cannot be detected.
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Page 14: Using The Device
3 USING THE DEVICE 3 Using the device 3.1 Activation and start of infusion 3.1.1 Preparations Insert the pointed tip of the IV line into the bottle in an upright posi- tion. Fill at most 1/2 of the drip chamber to keep the drip detection function operational. -
Page 15: Starting A New Treatment
3 USING THE DEVICE Note: Attaching different types of infusion sets to the Monidrop® W device must be done in accordance with the instructions. WARNING: Do not apply any force when attaching the drip chamber to the Monidrop® W device. If the fastening mechanism seems stiff, check that the position and installation of the infusion set and clamp is correct. -
Page 16: Notifications
4 NOTIFICATIONS 4 Notifications The Monidrop® W infusion monitor is equipped with its own notification system (notification sound and optic notification). Notificati- Notifi- Optic notification Acknowledg- on type cation ment Yellow Text/image tone Visual noti- Conti- Blinking Automatic fication nuous... -
Page 17: Battery Low
4 NOTIFICATIONS 4.1.2 Battery low The device gives notification with a blinking yellow light, a notification tone and a flashing triangle at the infusion rate symbol. The message is automatically cleared when the device is connected to the charger. • The device gives notification when the battery status is down to 10%. 4.1.3 Infusion rate is over 1200 ml/h The message is displayed with a flashing yellow light and sound and the screen displays a flashing notification triangle at the infusion rate symbol. -
Page 18: Battery Charge And Maintenance
100% The Monidrop® W infusion monitor can also be used when its battery is being charged, and it will operate normally. When the device is connect- ed to the charger, the middle LED at the top of the screen will be orange when the battery is being charged and the symbol shown below will be displayed in place of the battery status symbol. - Page 19 500 times before its capacity de- creases below 80% of the maximum value. • The battery will slowly discharge if the infusion monitor is not con- nected to the power grid and even if the device is not in use.
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Page 20: Cleaning
6 CLEANING 6 Cleaning Wipe the surface clean using a piece of cloth and a mild soap-water solu- tion. If required, disinfect the device using ApoWipe or a similar product. The device can also be disinfected as follows: • 80% isopropanol •... -
Page 21: Warranty / Inspection And Maintenance / Training
7 WARRANTY / INSPECTION AND MAINTENACE / TRAINING 7 Warranty / Inspection and maintenance / Training The manufacturer’s liability The manufacturer, assembly or installation company or importer is only responsible for device safety when: • An authorised person has installed the device or made expansions, additions, modifications or repairs. - Page 22 (the serial number in the image is an example and does not corres- pond to the correct serial number of the device) Training Training for the use of the Monidrop® W infusion monitor is available. Contact the device seller for more information.
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Page 23: Content Of The Delivery And Inspecting The Content / Recycling
8 Content of the delivery and inspecting the content / Recycling Content of the delivery Monidrop® W infusion monitor, charger, quick user guide Inspecting the content of the delivery Regardless of protective packaging, there may be transportation damage. Check that nothing is missing from the delivery. Do not use the device if it is damaged. -
Page 24: Technical Specifications
9 Technical specifications Device type Infusion monitor Classification (according to Internally powered medical device. Charger and device complies with class II requirements EN 60601-1) while connected to mains supply. Class (Directive 93/42/ EEC) Moisture protection Monidrop® W IP 52 (dustproof, protection... - Page 25 9 TECHNICAL SPECIFICATIONS Storage conditions: • 20 % … 85 % (of air humidity condensation) Relative humidi- ty, % -20 … +55 °C • Temperature 80 kPa … 106 kPa • Air pressure Battery type Li-ion-polymer Operation time Approx. 72 hours Charge time Approx.
- Page 26 9 TECHNICAL SPECIFICATIONS Manufacturer's instructions and declaration of electromagnetic com- patibility Disturbance test Compatibility Electromagnetic environment – in- structions RF emissions Group 1 Monidrop® W only uses RF energy in internal functions. Therefore, it only has very low emissions, and prob- CISPR 1 1 ably does not disturb any nearby electrical devices.
- Page 27 The Monidrop® W infusion monitor is intended for use in the electromagnetic environments defined below. The owner or user of the Monidrop® W infusion monitor and its parts must ensure that the device is used in such an environment.
- Page 28 9 TECHNICAL SPECIFICATIONS Note 1: Different testing values of standard IEC 60601-2-24 are indicated in the table. These testing values do not permit any hazardous interference, while interference is permitted using the lowest testing values of standard IEC 60601-1-2. Magnetic field at IEC 60601-2-24: 400 A/m Magnetic fields at a network...
- Page 29 Recommended distance between mobile and movable RF com- munications devices and the Monidrop® W infusion monitor The Monidrop® W infusion monitor is intended for use in electromagnetic environments where radiated RF emissions are controlled. The owner or user of Monidrop® W and its parts can help to prevent electromagnetic inter- ference by keeping the minimum distance between mobile and movable RF communications devices (transmitters) and Monidrop®...
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Page 30: Operating Instructions For Accessories
The Monidrop® W infusion monitor can only be charged using the charg- er delivered with the package. Always check that the correct charger is used. - Page 31 10 OPERATING INSTRUCTIONS FOR ACCESSORIES Do not operate where aerosol (spray) products are being used or where oxygen is being administered. The socket-outlet should be installed near the power supply and should be easily accessible. Do not unplug by pulling on cord. To unplug, pull on the plug, not on the cord.
- Page 36 MONIDOR Monidor Oy Version number 3.0 Elektroniikkatie 3 Approved: 6/2/2020 90590 Oulu Finland +358 10 31 15 860 www.monidor.com...
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