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Spirobank II

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Rev.1.6 

Page 7 of 35 

User manual 

 

WARNING  

Incorrectly applied oximetry sensors or damaged cables may cause inaccurate readings. Using a damaged oximetry sensor 
may cause inaccurate readings, possibly resulting in patient injury or death. Inspect each oximetry sensor before use. 

 

If an oximetry sensor appears damaged, do not use it. Use another oximetry sensor or contact your authorized repair center 

for assistance. 

 

Use only MIR oximetry sensors supplied with, or specifically intended for use with Spirobank II. Use of oximetry sensors not 
intended for use with the Spirobank II may cause inaccurate readings.

 

Oximetry measurements may be inaccurate in the presence of high ambient light. Shield the sensor area (with a surgical 
towel, for example) if necessary.  

 

 

WARNING 

Dyes introduced into the bloodstream (for example; to perform a diagnostic tests) such as methylene blue, indocyanine green, 
indigo carmine, patent blue V (PBV), and fluorescein may adversely affect the accuracy of the oximetry reading.  

 
Any condition that restricts blood flow, such as the use of a blood pressure cuff or a device for systemic vascular resistance, 
may cause the inability to determine accurate pulse rate and SpO2 readings. 
Remove  fingernail  polish  and/or  false  fingernails  before  applying  SpO2  sensors.  Both  may  cause  inaccurate  oximetry 

measurements. 
 
Significant  levels  of dysfunctional hemoglobins, such  as carboxyhemoglobin  or  methemoglobin, may adversely  affect the 
accuracy of the oximetry measurement. 

 
Optical cross-talk can occur when two or more sensors are placed in close proximity. Optical cross-talk may adversely affect 
the accuracy of the oximetry readings. The danger can be eliminated by covering each site with opaque material. 

Obstructions or dirt on the sensor’s emitter and/or detec

tor may cause a sensor failure or inaccurate readings. Make sure 

there are no obstructions and the sensor is clean. 
 
Autoclaving, ethylene oxide sterilizing, may cause sensor damage. Do not attempt to sterilize the sensor. 
 

Unplug the sensor from Spirobank II before cleaning or disinfecting to prevent damaging sensor or device, and to prevent 
safety hazards for the user. 

 

1.2.5

 

USB connection cable 

 

Incorrect use or application of the USB cable may produce inaccurate measurements, wich will show very  inaccurate values of  the 

patient’s condition. Carefully inspect each cable before use.

 

Do not use cables that appear to be or are damaged. If a new cable is required, contact your local distributor. 

Use only cables supplied by  MIR,  specifically designed to be used with  Spirobank II. The use of  other types of  cables  can lead to 
inaccurate measurements. 

 

1.2.6

 

Device 

 

 

WARNING 

The maintenance operations detailed in this manual must be fully and accurately carried out. If these instructions are not 
followed this may cause measurement errors and/or an incorrect test interpretation.  

Do not modify this equipment without authorization of the manufacturer. 
Any modifications, adjustments, repairs or reconfigurations must be made by the manufacturer or by personnel authorised 
by the manufacturer. Never attempt to make a repair on your own. The set-up of configurable parameters should only be 
made by qualified personnel. However, an incorrect set-

up of the parameters in no way endagers the patient’s health.

 

Technical description indicates, manufacturer will provide circuit diagrams, component part lists, descriptions, calibration 
instructions to assist to service personnel in parts repair. 
 
The  use  of  accessories  and  cables  other  than  those  specified  by  the  manufacturer  may  result  in  increased  emissions  or 

decreased immunity of the device.  
Spirobank II should not be used adjacent to or stacked with other equipment and if adjacent or stacked use is necessary, 
Spirobank II should be observed to verify normal operation in the configuration in which it will be used. 
If the device is connected to other instruments, to satisfy the safety requirements of the system required by the standard CEI 

EN 60601-1, it is necessary to use exclusively devices compliant to the safety standard. Therefore the PC or the printer which 
the Spirobank II is connected must be compliant to the standard CEI EN 60601-1. 
To dispose of the Spirobank II, the accessories, any plastic consumable materials (mouthpieces) as well as the battery, use 
only appropriate containers or return all such parts to the dealer or to a recycling center. All applicable local regulations must 

be followed.  

Summary of Contents for Spirobank II

Page 1: ...Spirobank II Rev 1 6 Page 1 of 35 User manual Spirobank II User manual rev 1 6 Issue date 20 01 2021 Approval date 20 01 2021...

Page 2: ...HE Spirobank II 17 2 1 Switch on and switch off the device 17 2 2 Energy saving 18 2 3 Main screen 18 2 4 Symbols and Icons 18 2 5 Service menu 19 2 5 1 Reusable turbine calibration 22 2 6 Patient Dat...

Page 3: ...al packaging In the unlikely event that you have a problem with your device please use the original packaging and return it to the distributor or manufacturer Should this be the case please follow the...

Page 4: ...he patient by the doctor WARNING The manufacturer cannot be held responsible for any damage caused by the user of the device failing to follow instructions and warnings in this manual If the user of t...

Page 5: ...Spirobank II is continuously checked during manufacturing and therefore the product complies with the established security levels and quality standards laid down by the Council Directive 93 42 EEC for...

Page 6: ...spirometer are only to be used as a reference guide to purchase the correct size mouthpiece required These mouthpieces are clean but not sterile To purchase appropriate mouthpieces generally either pa...

Page 7: ...vent safety hazards for the user 1 2 5 USB connection cable Incorrect use or application of the USB cable may produce inaccurate measurements wich will show very inaccurate values of the patient s con...

Page 8: ...may be damaged or suffer a drop in overall performance The internal battery pack safety sensor could also be damaged as well by any of the above events Furthermore the user of the device could be har...

Page 9: ...device or the battery charger and do not use it any longer as any of these events may cause acid leakage overheating smoke breakage and or fire NOTE The battery pack includes an internal safety protec...

Page 10: ...ed against vertically falling drops of water Antenna symbol for devices that include RF transmitters FCC ID FCC Identification code indicating traceability to FCC compliance Rx ONLY Reference to US FD...

Page 11: ...ielectric breakdown ESD can be caused by a buildup of static electricity by tribocharging or by electrostatic induction At lower relative humidity as the environment is drier charge generation will in...

Page 12: ...nt to the next to ensure the maximum level of hygiene and safety For a correct interpretation of a spirometry test the measured values must be compared either to the so called normal or predicted valu...

Page 13: ...y Flow at 75 of FVC L s FEV05 Volume expired after 0 5 seconds L FEV05 FEV05 FVC x 100 FEV075 Volume expired after 0 75 seconds L FEV075 FEV075 FVC x 100 FEV2 Volume expired in the first 2 seconds of...

Page 14: ...usable soft sensor for adults Reusable paediatric soft sensor Range SpO2 Arms Range SpO2 Arms Range SpO2 Arms 70 100 1 19 70 100 1 470 70 100 1 390 70 80 0 554 70 80 1 626 70 80 1 851 80 90 1 32 80 90...

Page 15: ...octor 1 6 3 Oximetry alarms description Spirobank II is equipped with audio and visual alarm indicators to alert the operator to provide prompt patient attention or to abnormal device conditions Spiro...

Page 16: ...h of the above mentioned oximetry sensors is used 1 6 4 Other features Memory Memory capacity for over 10000 spirometric tests The precise number depends on the individual configuration so it cannot b...

Page 17: ...discharge protection 8kV contact 15kV air Magnetic field immunity 30 A m Radio Frequency Immunity 3V m 80 2700 MHz MIR will make available on request circuit diagrams component part lists description...

Page 18: ...displayed with a reduction of the indicators 2 3 Main screen On the main screen the following areas can be accessed patient data management area spirometry area oximetry area archive area archive are...

Page 19: ...e key and then the key The service menu shows the following list of items Change date time LCD settings Bluetooth settings Select language Delete memory Select standard Select predicted Select turbine...

Page 20: ...standard to be used ATS ERS or NHANES III with the keys and then press the setting takes effect and the device returns to the Service Menu WARNING If the NHANES III standard is selected it is not pos...

Page 21: ...hreshold or rise above the maximum threshold of the SpO2 and BPM values previously set Use keys and to decrease increase the values and select moving the arrow with the keys and At the end press to re...

Page 22: ...g of the turbine is necessary The disposable turbine is check before the application of the external packaging for this reason it doesn t requires a periodic calibration If a calibration must be perfo...

Page 23: ...robank II is calibrated correctly then the FVC syringe value will be 3 00 FVC x 1 026 BTPS 3 08 L FVC at BTPS If the ambient temperature is 20 C the FIVC syringe value will be 3 00 FIVC x 1 102 BTPS 3...

Page 24: ...en without modifying any data WARNING A new patient is not created from the previous patient when selecting this function Patient info however can be modified Future tests will be associated to the pa...

Page 25: ...efault settings of the PC software will be transferred to the device and will remain in the device even when used in stand alone mode for example when the Spirobank II is connected to the PC and the u...

Page 26: ...results of the best test To end the test press During the test the Spirobank II emits beeps the frequency of which are directly proportional to the inspired and expired velocity of the air This helps...

Page 27: ...rst screen displays a Flow Volume graph of the Forced Vital Capacity pressing it is be possible visualize the best value of FVC FEV1 FEV1 and PEF with the percentage change compared to the predicted v...

Page 28: ...argest FVC is 100 mL 2 11 Oximetry Testing WARNING Check if the oximetry function is available in the device this function is an option in some models This is not available in BASIC version WARNING Th...

Page 29: ...the Spirobank II timer resets itself and the device starts recording data For any type of oximetry test if the sensor is not properly connected the following message will be displayed on screen after...

Page 30: ...ct to biocompatibility tests Choose an application site on the patient s finger or toe where the light source will be directly over and in line with the detector The preferred sites are the forefinger...

Page 31: ...manage Spirobank II The user can perform on line wireless tests of spirometry or oximetry and the tests will be directly stored in the database of winspiroPRO software 3 2 PC connection via USB port W...

Page 32: ...liquid solution and shake it so as to remove any impurities Leave the turbine immersed for the time specified in the instruction of the solution WARNING To avoid irreparable damage to the reusable tur...

Page 33: ...an the sensor WARNING Do not sterilize by irradiation steam or by using ethylene oxide Unplug the sensor from the device before cleaning or disinfecting it The sensor included with the Spirobank II is...

Page 34: ...t was not performed correctly Repeat the test and follow closely the indications shown on the screen Certain spirometry and or oximetry parameters are not shown at the end of a test Personalized param...

Page 35: ...n If the product is utilised differently from the use described in the User s Manual If any alteration adjustment modification or repair has been carried out by personnel not authorised by the manufac...

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