Gima WRIST PULSE OXIMETER User guide

Gima S.p.A.
Via Marconi, 1 - 20060 Gessate (MI) Italy gima@gimaitaly.com - export@gimaitaly.com
PROFESSIONAL MEDICAL PRODUCTS
www.gimaitaly.com
PULSOXIMETRO DA POLSO WRIST OXIMETER
Manuale d’uso - User manual
ATTENZIONE: Gli operatori devono leggere e capire completamente questo manuale prima di utilizzare il prodotto. ATTENTION: The operators must carefully read and completely understand the present manual before using the product.
34340
Gima S.p.A.
Via Marconi, 1 20060 Gessate (MI) Italy
Made in China
M34340-IT-GB-Rev.3-09.19
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Instructions to User
Wrist Oximeter is a precision measuring device, please read the manual very carefully before using this device. Failure to follow these instructions may cause measuring abnormality or device damage.
Notes:
• The contents contained in this manual are subjected to change without prior notice.
• Information furnished by GIMA is believed to be accurate and reliable. How­ever, no responsibility is assumed by us for its use, or any infringements of patents or other rights of third parties that may result from its use.
Instructions for Safe Operations
Check the device to make sure that there is no visible damage that may affect user’s safety and measurement performance. When there is obvi­ous damage, stop using the device. Necessary servicing must be performed by qualied service engineers ONLY. Users are not permitted to maintain it by themselves. The oximeter cannot be used together with the devices not specied in User Manual.
Cautions
Explosive hazard—DO NOT use the oximeter in environment with in­ammable gas such as some ignitable anesthetic agents. DO NOT use the oximeter while the testee is under MRI or CT scanning.
Warnings
For individual patients, there should be a more prudent inspecting in the placing process. The device can not be clipped on the edema and tender tissue. The light (the infrared light is invisible) emitted from the sensor is harmful to the eyes, so the user or even the service engineer should not stare at the light emitting components. To dispose the device, the local law should be followed.
Attentions
Keep the oximeter away from dust, vibration, corrosive substances, ex­plosive materials, high temperature and moisture. The device should be kept out of the reach of children. If the oximeter gets wet, please stop operating it. When it is carried from cold environment to warm and humid environ­ment, please do not use it immediately. DO NOT operate the button on front panel with sharp materials. High temperature or high pressure steam disinfection to the oximeter is not permitted. Refer to related chapter for instructions of cleaning and disinfection.
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1 OVERVIEW
1.1 Appearance
2 1 3
Figure 1 Front View
1. LCD screen
2. Set Key “¢”: shift display modes, conrm the operation etc.
3. Scroll Key “p”: Short Press to move display cursor, modify parameter values etc.
Long Press to choose display always on or not which will be effective during
measurement.
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6
Figure 2 Frontal Side View
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4. Buzzer
5. Data interface
6. Wristband
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Figure 3 Right Side View
7. SpO2 probe receptacle
1.2 Name and Model
Name: Wrist Oximeter Model: 34340
1.3 Conformation
It comprises the main unit and SpO2 probe.
1.4 Features
Wrist Oximeter can be used to measure and record the functional oxygen satu­ration (SpO2) and pulse rate accurately. Simply put your nger into sensor, SpO2 value and pulse rate value will be displayed on screen and stored in the device.
• It is light weight, small in size and easy to carry;
• Color OLED display;
• Perfusion index (PI) display is available;
• Automatic starts to measure SpO2 and Pulse Rate (PR);
• Real-time clock display and setting;
• Over-limit alert by audible beep, visible display and vibration of the oximeter, the over limits can be adjustable;
• It is convenient for you to measure SpO2 and pulse rate in long-term while sleeping or at other daily activity;
• Recording interval can be selected, up to 480 hours data memory;
• Applicable for longtime continuous measurement;
• PR trend curve and SpO2 trend curve view
• Data storage and transmission to PC for view and analysis.
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1.5 Intended Use
This Wrist Oximeter is intended for measuring the pulse rate and functional oxygen saturation (SpO2). It is applicable for long-term measurement of adult’s SpO2 and pulse rate in home and clinics.
2 BATTERY INSTALLATION
Figure 4 Battery Installation
1. Lift up the cloth covered on the battery cover. Then, use your index nger and middle nger to press against the battery cover. Meanwhile, slide it towards the side with SpO2 probe (as shown in Figure 4).
2. Refer to Figure 4, insert two AAA size batteries into the battery compartment properly in the right direction.
3. Replace the cover.
Remark: After nishing battery installation, the oximeter will automati­cally power on and display software version number rstly. Please take care when you insert the batteries, as the improper insertion may make the device not work.
3 OPERATION
NOTE for key button operation: Long pressing: press a key down more than 1 second. Short pressing: press a key down then let it go immediately (less than 1 second). The following methods can activate the device while it is in standby status:
1. Short press Set Key “¢” to activate the screen display.
2. Insert nger into the probe to activate the measurement and screen display automatically.
3. When USB data cable is connected between the device and PC, it will enter data uploading mode.
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NOTE: If the calendar clock time has not been set, the device will enter the Time
Settings screen while it powers up. The device will enter standby status automatically if there is no key-press and no measuring signal in 20 seconds. That is the only way to turn it off (i.e. at standby status).
3.1 Taking Measurement
1. Insert the SpO2 probe connector into the SpO2 probe receptacle on the de­vice properly.
SpO2 probe connector
Figure 5 SpO2 Probe Connection
2. Fix the oximeter on your left wrist (Figure 6);
Fingertip sign
Figure 6 Placement Illustration
3. Then, hold the probe with its opening towards your index nger. The probe should be oriented in such a way that the sensor side with a nger tip icon is positioned on the top (Figure 6).
4. Next, insert your index nger into the probe until the ngernail tip rests against the stop at the end of the probe (Figure 7). Adjust the nger to be placed evenly on the middle base of the sensor (make sure the nger is in the right position). If the index nger cannot be positioned correctly, or is not available, other nger can be used.
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Figure 7
Wrong Placement of the Probe:
Finger out Not deep enough Figure 8
5. The oximeter will automatically start measurement in 2 seconds. Then the default screen will be displayed (Figure 9A). User can read the values and view the waveform from the display screen.
Figure 9A Default Screen Display
“SpO2: SpO2 label; “99”: SpO2 value;
“PR”: Pulse rate label; “65”: Pulse rate value
• “ ”: Pulse beat icon;
• “ ”: Battery indicator;
• “ ”: Pulsation bar-graph;
• The displayed waveform is plethysmogram.
Key Operations::
• Short press “¢” key to switch display modes circularly, display screen will be switched among the three measure screens displays as shown in Figure 9A, Figure 9C and Figure 9D.
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• Long press “p” key: choose display always on or not which will be effective during measurement. If you choose display always on, the icon (“”) for “dis­play always on” will appear on the screen as shown in Figure 9B.
• Short press “p” key during measurement, the screen display direction can ip 180°.
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Figure 9B “Display Always On” is enabled
• “”: Icon for display always on, it indicates that the screen display is al­ways on during measurement. If the icon is disappeared, it indicates that the screen display will be off after a period of displaying time during measure­ment for power saving.
• “PI%”: Perfusion index label;
Figure 9D Real Time Clock
Figure 9C
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• “12:30”: the current time.
• “REC: 00:02:22”: the time period up to now in hh:mm:ss format for the cur- rent storing record since it was started. When nger is out, recording stops and here displays the time period for the last stored record. The time period will restart timing if a new piece of record is created once you insert nger into the probe to start another measurement.
Key Operations:
• Long press “¢” key, menu screen will be displayed, refer to section 3.2 for details;
6. Prompt information
• During measurement, if you haven’t inserted your nger into the probe or the probe is off, “Finger out ” will be prompted on the screen.
• During measurement, if the probe is not connected to the oximeter, “No Sig­nal!” will be prompted on the screen, as shown in Figure 10
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Figure 10 “No Signal” Indication
• During measurement, if the memory is full or the total number of the records reaches to 1024 pieces, the earliest record will be overwritten and the icon “ ” will appear on the screen for prompt, as shown in Figure 11.
Figure 11 When Memory is Full
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“ ”: Wireless icon; If the wireless (bluetooth communication) function is ena­bled, the icon will be displayed on screen. Please refer to chapter 3.2.5 Wireless Setting.
Note: It is suggested that the data shall be uploaded to computer when memo­ry is full, or the earliest record will be overwritten.
Working Mode
• The measurement will start automatically when the nger is inserted into the SpO2 probe, so the data recording (SpO2 and PR value) starts simultaneously as well. The display is as shown in Figure 9A.
• During measurement, if the icon “” (for “display always on”) is not shown on screen and no key button operation for 30 seconds, the screen display will be blank for power saving even when the measurement and data recording are still undergoing, but short pressing any key will activate the display for viewing the current measuring information again.
• If there is no signal and no key press to be detected (e.g. nger off) for 20 seconds, the device will be at standby status (i.e. blank screen and standby for measurement).
• When the device is at standby status, short pressing any key will activate the screen to default display screen, or once the nger is inserted in the SpO2 probe, the measurement will start and screen display will be activated as well.
Note: During measurement, there is a green-dot ashing on the screen for in­dicating the measurement and data recording are undergoing when the display screen is blank, and if SpO2 or/and PR values exceed the preset limit, it will activate the display and the value exceeded limit will ash.
3.2 Menu Operation
On display screen, long press “¢”, key menu screen will be displayed on the screen, as shown in Figure 12.
Figure 12 Menu Screen
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Review: view SpO2 and pulse rate trend graph;
Delete Data: delete all the records.
Alert: set SpO2 low limit, pulse rate high/low limit; and enable or disable the alert function.
Time: set current date and time;
Wireless: set or unset wireless function;
Rec Interval: set the time interval to record SpO2 and pulse rate data;
Pulse beep: set the pulse beep, enable or disable it.
Operation Instructions:
• Short press “p” key: shift cursor circularly;
• Short press¢” key: conrm the selection and enter into the corresponding screen;
Long press “¢ key: go back to the default screen display.
3.2.1 Trend Review
On menu screen, select “Review” and press “¢” key to enter Trend Review screen, as shown in Figure 13.
Figure 13 Trend Review Screen
“03/06/2008”: date of the measurement
“11:20:35”: start time of trend graph displayed on this screen;
¢p”: Page scroll (backward/forward) button;
Curves in the middle area:
Green curve: indicate pulse rate trend curve; Orange curve: indicate SpO2 trend curve;
Operation Instructions:
• Short press “p” key: Page scroll forward;
• Short press “¢” key: Page scroll backward;
• Long press “¢” key: go back to the menu screen;
Note: when the display screen is menu screen or its submenu screen, the measurement will be interrupted.
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3.2.2 Delete Data
On menu screen, select “Delete Data” and press “¢” key to enter into Deletion Conrmation screen. Then, select “Yes” with “p” key (short time press), after short pressing “¢” key, all the records will be deleted.
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Figure 14 Delete Records
3.2.3 Over-limit Alert Settings
On menu screen, select “Alert” and press “¢” key to enter Alert Limit Settings screen, as shown in Figure 15.
Figure 15 Over-limit Alert Settings
SpO2 Lo: set SpO2 low limit; Setting range:85%~100%, default setting: 85%;
PR Lo: set pulse rate low limit; Setting range:25bpm~99bpm, default setting: 50bpm;
PR Hi: set pulse rate high limit; Setting range: 100bpm~250bpm, default set­ting: 120bpm;
Alert: enable/disable the function of over-limit alert by audible beeping, visual display and vibration of the oximeter.
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If select “ON”, when SpO2 value or/and PR value exceeds its/their preset limits during measurement, the oximeter will beep and vibrate, and the numerical val­ue exceeded limit will ash.
• Sensor alert: enable/disable the alert function. The factory default is “OFF”. If select “ON”, when probe off and/or nger out, the oximeter will beep and vibrate, then pressing any key will mute it and stop vibrating.
Operation Instructions:
Short pressp” shift cursor circularly;
Short press¢” active the option;
Short presspkey: increase numerical value one time;
Long pressp key: increase numerical values continuously;
Short press¢key: conrm the selection;
Long press¢ key: go back to the menu screen;
3.2.4 Time Settings
On menu screen, select “Time” and press “¢” key to enter Time Settings screen, as shown in Figure 16.
Figure 16 Date and Time Settings
Date format: MM/DD/YYYY;
Time format: hh:mm:ss;
Operation Instructions:
• Short presspkey: shift cursor circularly;
Short press¢key: active the option;
Short presspkey: increase numerical value one time;
Long presspkey: increase numerical value continuously;
Short press¢key: conrm the modication;
Long press¢key: go back to the menu screen;
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3.2.5 Wireless Setting (Optional)
On menu screen, select “Wireless” and press “¢” key to enter Wireless Setting screen, as shown in Figure 17.
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Figure 17 Wireless Setting Screen
Select “ON” or “OFF” with “p” (key (short press), then short press “¢” key to conrm the selection. If you select “ON”, bluetooth communication will be enabled and the wireless icon displays on the screen. Meanwhile the oximeter can communicate with the bluetooth enabled host device such as a smart phone which is running specic application software (APP) to receive the measured data (SpO2, PR values and plethysmogram etc.). Please refer to the user manual of relative application software.
NOTE: Only the bluetooth protocol version 4.0 or later is supported.
3.2.6 Record Interval Settings
On menu screen, select “Rec Interval” and press “¢” key to enter Record Inter­val Setting screen, as shown in Figure 18.
Figure 18 Record Interval Setting
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Operation Instructions:
Short press¢key: active the option;
Short pressp” key: select record interval; three options: “1s”, “4s” and “8s;
Short press¢key: conrm the selection;
Long press¢key: go back to the menu screen;
Note: The length of data record is constrained to at least 30 seconds, and the maximal length for one record is also limited to 60 hours (for 1 second interval), 240 hours (for 4 second interval) or 480 hours (for 8 second interval) respectively.
3.2.7 Pulse Beep Settings
On menu screen, select “Pulse beep” and press “¢” key to enter Pulse Beep Setting screen, as shown in Figure 19.
Figure 19 Pulse beep settings
The factory default is “OFF”; The latest setting status is that of you start the oximeter next time.
3.3 Upload Data
Before uploading the data to PC, please quit from the menu screen if you are doing the setup or trend view operation. Before uploading, connect the USB data cable between the oximeter and PC.
• Do the following operations by the instruction in “Oximeter Data Manager User Manual”, then the data uploading will be activated.
• Copy the data from the oximeter to PC (or other host device) as the oximeter will be mapped as a removable disk when it is connected to PC by USB data cable.
3.4 Low Battery Indication
If “ ” appears on the screen, it indicates that battery power is not enough, please change batteries. If you keep on using it, after a while the batteries are exhausted and the oximeter will be off
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4 ADDITIONAL ADVICE FOR OPERATION
• The nger should be put properly and correctly.
• Avoid shaking nger as possible as you can during measurement;
• Do not put wet nger directly into sensor.
• Avoid placing the device on the same limb which is wrapped with a cuff for blood pressure measurement or during venous infusion.
• Do not let anything block the emitting light from device.
• Electrosurgical device interference may affect the measuring accuracy.
• Using enamel or other makeup on the nail may affect the measuring accura­cy.
• If the rst reading appears with poor waveform (irregular or not smooth), then the reading is unlikely true, the more stable value is expected by waiting for a while, or a restart is needed when necessary.
5 TECHNICAL SPECIFICATIONS
A. Display mode: Color OLED Display B. Power supply requirement:
2 x LR03 (AAA) alkaline batteries or Ni-MH rechargeable batteries Supply voltage: 3.0 VDC Continues working time (display is off): >12hours
C. Operating current: ≤50mA D. SpO2 Parameter Specications
Transducer: dual-wavelength LED Measurement wavelength: Red light: 663 nm, Infrared light: 890 nm. Maximal optical output power: less than 1.5mW maximum average Measuring range: 35~100% Measuring accuracy: Not greater than 3% for SpO2 range from 70% to 100% *NOTE: Arms is dened as root-mean-square value of deviation according to ISO 9919.
E. Pulse Rate Parameter Specications
Measuring range: 30bpm~240bpm Accuracy: ±2bpm or ±2% (whichever is greater)
F. Preset limits:
SpO2 Low limit setting: 85% Pulse Rate limit setting range: Upper limit: 120bpm Lower limit: 50bpm
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G. Update rate:
6 seconds moving average for SpO2 and 8 beats average for Pulse Rate read­ings.
H. Perfusion Index Display
Range: 0.2%~20%
I. Performance under low perfusion condition
The accuracy of SpO2 and PR measurement still meets the specication de­scribed above when the modulation amplitude is as low as 0.6%.
J. Resistance to interference of surrounding light:
The difference between the SpO2 value measured in the condition of indoor natural light and that of darkroom is less than ±1%.
K. Resistance to 50Hz /60Hz interference:
SpO2 and PR are precise which have been tested by Fluke Biomedical Index 2 series SpO2 simulator.
L. Dimensions: W 59mm×D 49mm×H 22mm
Net Weight: about 60g (not including batteries).
M. Classication
The type of protection against electric shock: Internally powered equipment. The degree of protection against electric shock: Type BF applied part. The degree of protection against harmful ingress of liquids: IPX2. Electro-Magnetic Compatibility: Group I, Class B.
6 ACCESSORIES
• A data cable (optional)
• A Wristband
• A SpO2 Probe
• Two batteries (AAA)
• A User Manual
Note: The accessories are subject to change. See the items and quantity in your hand for detailed.
7 REPAIR AND MAINTENANCE
7.1 Maintenance
The service life (not a warranty) of this device is 5 years. In order to ensure its long service life, please pay attention to the maintenance.
• Please change the batteries when the low-voltage indicator lightens.
• Please clean the surface of the device before using. Use cloth with alcohol to wipe the device rst, and then let it dry in air or wipe it dry.
• Please take out the batteries if the oximeter will not be used for a long time.
• The recommended storage environment of the device: ambient temper-
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ature: -20ºC ~60ºC, relative humidity 10%~95%, atmospheric pressure: 50kPa~107.4kPa
• The oximeter is calibrated in the factory before sale, there is no need to cali­brate it during its life cycle.
However, if it is necessary to verify its accuracy routinely, the user can do the
verication by means of SpO2 simulator, or it can be done by the local third party test house.
High-pressure sterilization cannot be used on the device. Do not immerse the device in liquid.
7.2 Cleaning and Disinfecting Instruction
Surface-clean sensor with a soft gauze by wetting with a solution such as 75% isopropyl alcohol, if low-level disinfection is required, use a 1:10 bleach solution.
Then surface-clean with a damp cloth and dry with a piece of cloth.
• Clean the wristband with soapy water. Please detach the wristband from the oximeter rstly. (Refer to Appendix for detailed disassembly method).
Caution: Do not sterilize by irradiation steam, or ethylene oxide. Do not use the sensor if it is damaged.
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8 TROUBLESHOOTING
Trouble Possible Reason Solution
The
SpO2 and Pulse Rate display instable
Can not turn on the device
Fragmental trend curve of
SpO2
and PR
1. The nger is not placed far enough inside.
1. The batteries are drained or almost drained.
2. The batteries are not inserted properly.
3. The device is malfunctioning.
1. Your nger is out of proper location in the probe.
2. Blood ow in the nger blocked.
3. Extreme movement.
1. Place the nger correctly inside and try again.
1. Change batteries.
2. Reinstall batteries.
3. Please contact the local service center.
1. Adjust your nger location properly.
2. Make sure there is no object may occlude the blood ow.
3. Extreme movement may cause invalid measuring result.
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Trouble Possible Reason Solution
Always display “No Signal”
9 APPENDIX
A - Common Knowledge for SpO2 Measurement
1 Meaning of SpO2
SpO2 is the saturation percentage of oxygen in the blood, so called O2 concen­tration in the blood; it is dened by the percentage of oxyhemoglobin (HbO2) in the total hemoglobin of the arterial blood. SpO2 is an important physiological parameter to reect the respiration function; it is calculated by the following method: SpO2 = HbO2/ (HbO2 + Hb)×100% HbO2 are the oxyhemoglobins (oxygenized hemoglobin), Hb are those hemo­globins which release oxygen.
2 Principle of Measurement
Based on Lamber-Beer law, the light absorbance of a given substance is di­rectly proportional with its density or concentration. When the light with certain wavelength emits on human tissue, the measured intensity of light after ab­sorption, reecting and attenuation in tissue can reect the structure character of the tissue by which the light passes. Due to that oxygenated hemoglobin (HbO2) and deoxygenated hemoglobin (Hb) have different absorption character in the spectrum range from red to infrared light (600nm~1000nm wavelength), by using these characteristics, SpO2 can be determined. SpO2 measured by this oximeter is the functional oxygen saturation -- a per­centage of the hemoglobin that can transport oxygen. In contrast, hemoxime­ters report fractional oxygen saturation – a percentage of all measured hemo­globin, including dysfunctional hemoglobin, such as carboxyhemoglobin or metahemoglobin. Clinical application of pulse oximeters: SpO2 is an important physiological pa­rameter to reect the respiration and ventilation function, so SpO2 measure­ment used in clinical becomes more popularly, such as monitoring the patient with serious respiratory disease, the patient under anesthesia during opera­tion, premature and neonate. The status of SpO2 can be determined in time
1. The probe is not connect­ed to the oximeter properly.
2. The nger is not placed well.
3. The probe connector or the probe sensor is broken.
1. Connect the probe to the oximeter properly and try again.
2. Place the nger properly and try again.
3. Please contact the local service center.
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by measurement and nd the hypoxemia patient earlier, thereby preventing or reducing accidental death caused by hypoxia effectively.
3 Factors affecting SpO2 measuring accuracy (interference reason)
• Intravascular dyes such as indocyanine green or methylene blue.
• Exposure to excessive illumination, such as surgical lamps, bilirubin lamps, uorescent lights, infrared heating lamps, or direct sunlight.
• Vascular dyes or external used color-up product such as nail enamel or color skin care.
• Excessive patient movement.
• Placement of a sensor on an extremity with a blood pressure cuff, arterial catheter, or intravascular line.
• Exposure to the chamber with High pressure oxygen.
• There is an arterial occlusion proximal to the sensor.
• Blood vessel contraction caused by peripheral vessel hyperkinesias or body temperature decreasing.
4 Factors causing low SpO2 Measuring value (pathology reason)
• Hypoxemia disease, functional lack of HbO2.
• Pigmentation or abnormal oxyhemoglobin level.
• Abnormal oxyhemoglobin variation.
• Methemoglobin disease.
• Sulfhemoglobinemia or arterial occlusion exists near sensor.
• Obvious venous pulsations.
• Peripheral arterial pulsation becomes weak.
• Peripheral blood supply is not enough.
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B - Wristband Installation and Disassembly
Introduction
Velcro (1) Buckle Wristband Velcro (2)
Fig. A
One side of oximeter The other side of oximeter
Fig. B Wrist oximeter
Installation Procedure
Step 1: Insert the wristband to the oximeter from one side to the other side, as shown in Fig. C.
Fig. C
Step 2: Put the oximeter on the wrist, and stick the Velcro (1) to the inner side of wrist­band, press the wristband to make the Vel­cro (1) stick to the inner side of wristband rmly, as shown in Fig. D.
Fig. D
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Step 3: Bring the wristband out from the buckle, and fold back the wristband, as shown in Fig. E. Then press the Velcro (2) to make it stick to the outer side of wristband rmly, as shown in Fig. F.
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Fig. E Fig. F
Disassembly: The process of wristband disassembly is similar to the installation method, but with reverse procedure.
Note: Please detach the wristband from the oximeter before cleaning the
wristband.
C - DOWNLOAD APP SOFTWARE ONTO SMART PHONES
Terminal devices such as Android/iOS smart phones can be used to receive data from the Oximeter in real-time, store the received data, and also review the stored data. To use this function, download the corresponding APP software onto the smart phone device.
Please follow the procedure to down­load:
1. Scan the QR Code image in below Figure.
2. When successfully scanned, a web link for downloading the APP soft­ware will be displayed.
3. Open the web link to download the APP software.
4. Install the software when success­fully downloaded.
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Note: For smart phone or Pad with iOS system (such as iPhone, iPad), you can also search the APP software on Apple App Store, then enter “Shenzhen Cre­ative” into the search box. (if you use an iPad to search, please select “iPhone only” as well for searching.) Once the search results are listed, select the App name “@health” with icon , then download it from App software.
Key of Symbols
Symbol Description
%SpO2 Pulse Oxygen Saturation
PI% Perfusion Index
PR Pulse Rate
Wireless icon
USB interface
Pulse rate icon
Low battery voltage Icon for display always
on Full memory icon
Serial number
Date of manufacture
Manufacturer
Symbol Description
Type BF applied part
Follow instructions for use
WEEE disposal
Product code Medical Device complies
with Directive 93/42/EEC Lot number Caution: read instructions
(warnings) carefully
Keep in a cool, dry place
Keep away from sunlight
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Disposal: The product must not be disposed of along with other do­mestic waste. The users must dispose of this equipment by bringing it to a specic recycling point for electric and electronic equipment. For further information on recycling points contact the local authorities, the local recycling center or the shop where the product was purchased. If the equipment is not disposed of correctly, nes or penalties may be applied in accordance with the national legislation and regulations.
GIMA WARRANTY CONDITIONS
Congratulations for purchasing a GIMA product. This product meets high quali­tative standards both as regards the material and the production. The warranty is valid for 12 months from the date of supply of GIMA. During the period of validity of the warranty, GIMA will repair and/or replace free of charge all the defected parts due to production reasons. Labor costs and personnel traveling expenses and packaging not included. All components subject to wear are not included in the warranty. The repair or replacement performed during the warranty period shall not ex­tend the warranty. The warranty is void in the following cases: repairs performed by unauthorized personnel or with non-original spare parts, defects caused by negligence or incorrect use. GIMA cannot be held responsible for malfunction­ing on electronic devices or software due to outside agents such as: voltage changes, electro-magnetic elds, radio interferences, etc. The warranty is void if the above regulations are not observed and if the serial code (if available) has been removed, cancelled or changed. The defected products must be returned only to the dealer the product was purchased from. Products sent to GIMA will be rejected.
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