i . troubleshooting Message/icon Cause Solution SPO oF CHT TOD BRAY 1 CHEETOS Lac bares ng HA 64 Lal The amplitude of the pulse waveform is too low, or the sensor is not positioned correctly, Check that the light emitting and receiving parts of the sensor LED are aligned. Spud CHITCHAT The expiration date of the sensor is approaching. Replace the probe. For the expiration date of the sensor, refer to “6. Sp Oz Monitoring/About the Expected Life of Asimov Sensors”. The Spot measurement is muted OFF.
sig Lad 11. Troubles ii poling Situation Cause Solution Sp Oz value is The probe size is Use a probe, which fits unstable. improper. properly. The probe is peeling off or is affected by the outside light due to the poor Attach the probe properly following the instruction. condition Transmitting and measuring LED are dirty. sensor dirt. Clean both LED sensors from Details of the “Electrode” Message The following “Electrode?” messages are displayed depending on the selected lead cable and lead.
i . troubleshooting min Case of Dropping the into Water in case of dropping the into water containing disinfectant, pick up the as soon as possible. in case of dropping the equipment into dirty water, clean it without disconnecting the ECG lead cable and Spoor probe (sensor), and make sure that the battery compartment lid is locked. After cleaning, wipe off any moisture thoroughly before removing the ECG lead cable, SpO: probe (sensor), or batteries. /CAUTION @ Do not use a dryer.
Le 12. Cleaning and Disinfection The cleaning and disinfection of the ECG lead cable, and Sp Oz probe {sensor) shall be performed as follows. CAUTION Do not sterilize the ECG lead cable, and Sp0» probe (sensor) in any manners, such as radioactive rays, steam, or ethylene oxide. e Cleaning the Housing 1. Clean the equipment using squeezed gauze or an absorbent cotton cloth dampened with alcohol. When cleaning, do not allow any solution to enter the equipment or connectors.
12. Cleaning ar sig Lad d Disinfection s Cleaning the Connector Do not wipe the ECG connector and Spoor connector with a swab, gauze, or absorbent cotton. Use an air duster to clean the dust and dirt in the connector. MA CAUTION if a swab, gauze, or cotton is used to clean the connector, dust or cation fibers may enter the connector causing inadequate contact. Also, chemical solution may enter the connector causing inadequate contact.
Le 13. Maintenance and Inspection This section explains the daily checks and periodic checks of the To ensure safely, reliability, and high performance, a “Daily Check” and “Periodic Check” must be performed. We are not liable for any accident arising from lack of maintenance. A full technical description of the is available from your local Fukuoka Dens hi representative. CAUTION ® Do not open the housing. @ Do not allow excessive moisture or cleaning agents into the connectors or inside the equipment.
Li 13. Maintenance and Inspection Soe Daily Check List No Inspected Date Inspected by Location Davits Gyps. Si No. hags Oms Details Criteria Judgment Visually check for any damage, i" . Appearance cracks, chip, peeled label, and Ha ab normality shooed be oOK/ olG loosen screw on the housing. Visually sack for the ring No damage, kink, floating, condition of the battery and adhesion of dust oi ONG compartment lid should be found. Foes .
u Periodic Check 13. Maintenance and Inspection The periodic maintenance check is intended to check the medical equipment used daily in a medical institution to prevent failures and accidents and to ensure safety and reliability. The check procedures are described for daily and periodic checks. Each sack item must be performed according to the described check procedure. The consignee can select the check items according to the product quality, frequency of usage, and maintenance check period.
sig Lad 13. Maintain ii Le ce and inspection No | Check tem Check Procedure Criteria 3. Display, Operation 01 Labels Visually check the labels, Should be clean, clear caution labels, sfc. and firmly attached. 02 | Operation, Check by operating the Should operate Switches and switches and keys. properly. keys 03 | Display Check that the characters and | The characters and waveform appear on the waveform should be display. clearly displayed. The brightness should be sufficient.
13. Maintenance and Inspection No | Check tem Check Procedure Criteria 06 ECG Sensitivity | With comprehensive tester, Wave form size on the apply mV voltage and receiving monitor measure the displayed should be within 0mm amplitude. +10% at sensitivity 1. According to test procedures of IEC 60601-2-27: 2011 201.121.1011 07 | Heart Rate With ECG simulator, test For reference Accuracy” heartbeat 60, 180 beats/min, heartbeat signal of 60, and check the displayed HR 180 beats/min, error value.
sig Lad 13. Maintain ce and inspection * As these functions are dependent on the design or software, these items are not mandatory for periodic checks. Perform the test as necessary. No | Check tem Check Procedure Criteria 6. Arterial Oxygen Saturation (Spousal) 01 Spot Accuracy | Measure the error at 75%, Error should be within 90% using a Spoor simulator. +2% for Spa of 70100%. Prepare other reference Emory between the 2 device, perform measurement | devices should be on healthy subject, and within 24%.
. Maintenance and Inspection No | Check tem Check Procedure Criteria 03 | Leakage current | Measure the leakage current Leakage current when when external when external voltage is external voltage is voltage is applied to the patient applied to the patient applied to the connection in the Type F connection in the Type patient attaching part using a leak F attaching part. {SFC} connection in measurement safety tester. 50.05mA.
13. Maintenance and Inspection Le u Repairing the Equipment This equipment is basically repaired at Fukuoka Dens hi factory. if detailed information about the repair is needed, contact Fukuoka Dens hi. On-site repair is possible for the following parts. + Replacing the battery compartment lid CAUTION Make sure to replace the parts correctly. Otherwise, it may cause damage and heat generation of the equipment.
13. Maintenance e Tools ce and inspection + Phillips screwdriver (#0) e Assembly and Disassembly Follow the procedure below to remove the battery compartment lid unit. 1. Remove the label. 2. Remove the 2 installation screws, then remove the battery compartment lid unit.
Le 13. Maintenance and Inspection Follow the procedure below to attach the battery compartment lid unit. 1. Set the battery compartment lid unit adjusting to the front case. 2. Secure the battery compartment lid unit with new 2 installation screws. Make sure that the screws are securely tightened.
fi ith Maintenance and inspection 4. Attach the label firmly aligning with the groove of the battery compartment lid unit.
Le 14. Standard and Optional Accessories WARNING Use only the accessories specified by Fukuoka Dens hi for the LX-8300M Otherwise, the cannot deliver its maximum performance and may be damaged, resulting in a safety hazard. CAUTION For quality improvement, specifications are subject to change without prior notice. s Standard Accessories item Mode! Type ty Remarks AHA color code, electrode ECG lead | GMT026TH.
14. Stands a 7% sig Lad ii Sp0; Sensors » INCS Sensor nd Optional Accessories INCS Neo-L.
i 14. Accessories and optional Accessories Sask When using the RD SET Sensor, the following conversion cables are required.
Le 15. Specification a Specification AN CAUTION For quality improvement, specifications are subject to change without prior notice. General Size: mm x mm x mm {not including the protrusion) Weight: Approximately 180 g (with battledress) Transmitting Waveform: ECG 1CH or 2CH (select from the ECG lead cable), Respiration waveform, pulse waveform (with Spitz value) ECG Lead Cable Type: 3-electrodes, 4-electrode, or S-electrode (Limb+Chest) lead cable. Automatically detect the type by inserting the lead cable.
18.
Le ) : ‘Specification Sweep speed: 12.5 mm/s Heart rate 80 bpm Ventricular Ignominy: 80 bpm meter accuracy and response to irregular i Co rhythm: 60 bpm Ventricular Ignominy: 60 bpm 120 bpm Ventricular Ignominy: 120 bpm TY TINY yy 20 bpm Bidirectional Systoles: 80 bpm Aa A Respiration (impedance Method) Accuracy of Sensitivity: 10 mm/1G £2 mm {When standard Impedance is 4800.) Resp.
18. sig Lad Specifics ies NOTE The Sp: measurement accuracy is determined based on the values of the root-mean-square (rms) difference between Sp Oz readings of the pulse taximeter equipment and values of Saga determined with a CO-taximeter, by healthy adult volunteers.
Le ) Specification Transmission Method of Modulation Mode: Frequency: Oscillation Method: Channel Spacing: Occupied Frequency Bandwidth: RF Output Power: Transmitting Antenna: Safety General Standard: EMC Standard: The class of protection against electric shock: The type of protection against electric shock: Operating Environment Temperature: Humidity: Atmospheric Pressure: Digital, Frequency shift keying 1385 MHz to 1400 MHz, 1427 MHz to 1432 MHz PLL Synthesizer method by crystal control 25.
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