Operators Manual
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BioCon -900S OPERATOR’S MANUAL
CUBEScanTM BioCon-900S Operator’s Manual This page left blank intentionally.
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CUBEScanTM BioCon-900S Operator’s Manual
BioCon-900S Bladder Volume Measurement System
Operator’s Manual CAUTION : In the United States, federal Law restricts this device to sale by or on the order of a physician. “This product is not made with natural rubber latex.”
The information in this document is subject to change at any time without notice. No part of this document may be reproduced or transmitted in any form or by any means, electronic or mechanical, for any purpose, without the express written permission of Mcube Technology. Examples or images in this document are fictitious and do not in any way represent real patient data. For up-to-date user information, contact your local distributor or [email protected]. All other product or service names are the property of their respective owerner..
Mcube Technology Co., Ltd. #803 123, Bonghwasan-ro, Jungnang-gu, Seoul, Korea Tel: +82-2-3421-7780 Fax: +82-2-3421-7076 E-mail: [email protected] Web site: www.mcubetech.co.kr
Copyright ⓒ 2018 by Mcube Technology Co.,Ltd. All rights reserved.
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CUBEScanTM BioCon-900S Operator’s Manual
TABLE OF CONTENTS 1
GENERAL INFORMATION ... 6 1.1 1.2 1.3 1.4 1.5
2
SAFETY INFORMATION ... 8 2.1 2.2 2.3 2.4 2.5 2.6
3
PRODUCT DESCRIPTION ... 6 INTENDED USE / INDICATIONS FOR USE ... 6 PATIENT/USER CHARACTERISTICS ... 6 PRESCRIPTION STATEMENT... 6 SERVICE ... 6
NOTICE TO ALL USERS... 8 CONTRAINDICATIONS ... 8 BIOLOGICAL SAFETY ... 8 ELECTRICAL SAFETY ... 8 DEVICE SAFETY... 9 SAFE HANDLING PROCEDURES FOR TRANSPORTER ... 11
INTRODUCTION ... 12 3.1 3.2 3.3 3.4 3.5 3.6
PRODUCT FEATURES ... 12 SYSTEM COMPONENTS ... 12 OUTER APPEARANCE – PROBE ... 13 OUTER APPEARANCE - CHARGER ... 14 DISPLAY AND ICONS ... 15 ICON DIRECTORY ... 15
4. SETUP ... 18 4.1 4.2 4.3
5
HOW TO USE ... 20 5.1 5.2 5.3 5.4 5.5 5.6 5.7 5.8 5.9 5.10 5.11
6
CHECKUP BEFORE USE ... 20 TURN SYSTEM ON/OFF ... 20 SELECT PATIENT TYPE ... 21 RECORD INFORMATION FOR A PATIENT ... 22 MEASURE BLADDER VOLUME ... 24 DISPLAY A SCAN RESULTS ... 26 RE-AIM BLADDER ... 28 SAVE A SCAN RESULT ... 28 FETCH A MISSING DATA ... 29 FINISH THE MEASUREMENT ... 29 MANAGE SAVED SCAN RESULTS ... 29
SCREENS ... 32 6.1 6.2 6.3 6.4 6.5 6.6 6.7 6.8 6.9 6.10 6.11
7
ACCURACY OF MEASUREMENT ... 18 CHARGE THE BATTERY ... 18 SCAN TYPE... 19
HOME SCREEN ... 32 INFORMATION SCREEN ... 32 BARCODE SCREEN (OPTIONAL) ... 33 VIRTUAL KEYBOARD SCREEN ... 33 NORMAL SCAN SCREEN ... 34 PRE-SCAN SCREEN ... 34 SCAN RESULT SCREEN ... 35 REVIEW SCREEN ... 35 SETUP SCREEN ... 36 BATTERY STATUS ... 37 DIALOG BOXES... 38
SETTINGS ... 39 7.1 7.2
DATE FORMAT SETTINGS... 39 DATE SETTINGS... 39
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CUBEScanTM BioCon-900S Operator’s Manual 7.3 7.4 7.5 7.6 7.7
8
MAINTENANCE ... 43 8.1 8.2 8.3 8.4 8.5 8.6 8.7 8.8 8.9
9
TIME SETTINGS... 39 SLEEP MODE SETTINGS ... 40 DISPLAY BRIGHTNESS SETTINGS ... 40 PRE-SCAN SETTINGS ... 41 DELETE ALL MEASUREMENTS ... 41
TROUBLESHOOTING ... 43 DIALOG BOXES FOR MAINTENANCE... 43 CLEANING & DISINFECTION ... 44 BATTERY MAINTENANCE ... 46 WEEKLY INSPECTION ... 46 DISPOSAL ... 46 DEVICE REPAIR ... 46 SELF TEST ... 47 CALIBRATION ... 48
SPECIFICATIONS ... 51 9.1 9.2 9.3 9.4 9.5
ACOUSTIC OUTPUT TABLE ... 51 ELECTROMAGNETIC COMPATIBILITY ... 51 EXCESSIVE TEMPERATURE TEST RESULT ... 54 SPECIFICATIONS OF COMPONENTS ... 54 ENVIRONMENTAL CONDITIONS ... 56
10 GLOSSARY ... 58 11 SYMBOL DIRECTORY ... 59 12 REFERENCES ... 61
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CUBEScanTM BioCon-900S Operator’s Manual
1
GENERAL INFORMATION
1.1
PRODUCT DESCRIPTION
CUBEScanTM BioCon-900S is a safe and easy, non-invasive system to measure the bladder volume. The device consists of a probe, CUBEScan Charger, and various components. The probe is a B-mode instrument, hand-held, wireless and battery-operated. A 3D-mechanical sector transducer provides cross– sectional images of the bladder from up to 12 scan planes and bladder volume is calculated based upon those images and displays 12 scan planes on a screen. Furthermore, a live image of the bladder during Pre-scan makes it easier to detect the bladder before scanning. The CUBEScan Charger is used for recharge of the probe’s internal battery.
1.2
INTENDED USE / INDICATIONS FOR USE
CUBEScanTM BioCon-900S is a B-mode pulsed-echo ultrasound device. The BioCon-900S projects ultrasonic energy through the lower abdomen of a patient to obtain images of the bladder to calculate the urine volume non-invasively. BioCon-900S is intended to be used by a qualified medical professional to non-invasively measure the urine volume in the bladder. Contraindications for the BioCon-900S are fetal use and use on pregnant patients.
1.3 1.3.1
PATIENT/USER CHARACTERISTICS PATIENT POPULATION
1) Male (All other patients) 2) Female patient - A female who has not had a hysterectomy - A female who has had a hysterectomy 3) Pediatric patient; A child with height less than 47 inches (120cm) and weight less than 55 lbs (25kg)
1.3.2
USERS
1) Physicians 2) Medical Professionals
1.3.3
MEDICAL CONDITIONS INCLUDING TARGET GROUP AND DISEAS
Bladder volume measurement system measures bladder volume, and it provides the accurate data to aid in the diagnosis of common urological condition, to assess urinary retention, to help unnecessary catheterization and to reduce rates of catheter-associated urinary tract infection. The benefits are as below; BioCon-900S assists to; a. Assess urinary retention b. Evaluate post-operative urinary retention (POUR) c. Reduce unnecessary catheterization d. Reduce catheter-associated urinary tract infections(CAUTIs) e. Identify a blocked Foley catheter f. Evaluate the need to catheterize after Foley catheter removal g. Evaluate the need to catheterize during intermittent catheterization h. Support to train urination and self-cathererization i. Measure PVR (Post Void Residual)
1.4
PRESCRIPTION STATEMENT
Federal (United States) law restricts this system to sale by or on the order of a physician.
1.5
SERVICE
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CUBEScanTM BioCon-900S Operator’s Manual If you encounter difficulty with the system, please contact local distributers or Mcube Technology at [email protected]
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CUBEScanTM BioCon-900S Operator’s Manual
2
SAFETY INFORMATION
2.1
NOTICE TO ALL USERS
This guide covers components, function, maintenance, storage, and precautions needed to use this system. All users must read and thoroughly understand this entire guide prior to using the BioCon-900S. This section has information on safe use of the BioCon-900S (Biological Safety, Electrical Safety, Device Safety and Safe handling procedures for transporter). Complies with FDA performance standards for laser products except for deviations pursuant to Laser Notice No. 50, dated June 24, 2007.
2.2
CONTRAINDICATIONS
WARNING Do not use the BioCon-900S on following cases: 1) Fetal use or pregnant patients. 2) Patients with ascites. 3) Patients with open or damaged skin. Wounds in the suprapubic region.
2.3
BIOLOGICAL SAFETY
To date, exposure to pulsed diagnostic ultrasound has not been shown to produce adverse effects. However, ultrasound should be used only by medical professionals when clinically indicated, using the lowest possible exposure times possible commensurate with clinical utility. The ultrasonic output power of BioCon-900S is limited to the minimum level necessary for performance effectively. Data on acoustic output levels is listed in section “9. Specifications”.
2.4
ELECTRICAL SAFETY
This system meets IEC 60601-1, Class I, Type BF isolated patient-applied parts safety requirements. This system complies with the applicable medical device requirements published in the Canadian Standards Association (CSA), European Harmonized Standards, and Underwriters Laboratories (UL) safety standards. To avoid the risk of electrical shock or injury, observe the following warnings and cautions.
WARNING
To avoid the risk of electric shock, this device must only be connected to an adapter with the
protective earth. - Grounding reliability can only be achieved when device is connected to a receptacle marked “Hospital Only” or “Hospital Grade” or the equivalent. Do not operate the system in the presence of flammable gases or anesthetics. Do not use the device with any defibrillator at the same time. Do not use the device with any HF surgical equipment at the same time. Before using the system, inspect the enclosures, power cord and adapter.Do not use the system if these are damaged. Do not use the probe if the entire probe is accidentally immersed in solution. Connect only items that have been specified as part of the BioCon-900S or that have been specified as being compatible with the BioCon-900S. Charge the probe only with the provided Charger. Connect the Charger only to the provided adapter.
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CUBEScanTM BioCon-900S Operator’s Manual
Do not attempt to open the system components. This may cause serious injury to the operator or patients. All services must be made by a qualified technician only.
Use of components and cables other than those specified or provided by the manufacturer of this
device could result in increased electromagnetic emissions or decreased electromagnetic immunity of this device and result in improper operation. Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the BioCon-900S, including cables specified by the manufacturer. Otherwise, degradation of the performance of this device could result.
CAUTION
The BioCon-900S has been tested and found to comply with the electromagnetic compatibility (EMC) limits for medical systems to IEC 60601-1-2. These limits are designed to provide reasonable protection against harmful interference in a typical medical installation. Medical systems must be installed and operated according to the instruction in this manual. For more information, see the section “9.2 ELECTROMAGNETIC COMPATIBILITY”. This device is suitable for use in the professional health care environment Medical electric devices can be affected by portable or mobile RF communication devices. Turn off any portable or mobile RF device before operating your system. Electrostatic discharge (ESD), or static shock, is a naturally occurring phenomenon. ESD is common in conditions of low humidity, which can be caused by heating or air conditioning. Static shock is a discharge of electrical energy from a charged body to a lesser or non-charged body. The degree of discharge can be significant enough to cause damage to a transducer or an ultrasound system. The following precautions can help reduce ESD: anti-static spray on carpet, anti-static spray on linoleum, and anti-static mats. The EMISSIONS characteristics of this device make it suitable for use in industrial areas and hospitals (CISPR 11 class A). If it is used in a residential environment (for which CISPR 11 class B is normally required) this device might not offer adequate protection to radio-frequency communication services. The user might need to take mitigation measures, such as relocating or re-orienting the device. Do not use the system if an error message appears on the display: note the error code; call Mcube technology or your local distributor, shut down the system
2.5
DEVICE SAFETY
To protect your BioCon-900S, and components, follow these warnings and cautions.
WARNING
No modification of this device is allowed. Do not use the system if the head of probe is damaged. To avoid the risk of excessive heating or damage to the device, use the device in a well-ventilated environment.
To avoid damage to cables, do not excessively twist or bend cables associated with the device. Turn off the device and unplug the charger if it will not be used for a long period of time. Do not use the system if there is evidence of leakage of internal liquids. Wash hands immediately in warm, soapy water. In the event that LCD is damaged, care should be taken to avoid contact with liquid crystal. Take the urgent action indicated should any of the following situations arise: - If liquid crystal comes in contact with your skin, clean the area with a cloth and then wash thoroughly with soap and running water.
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CUBEScanTM BioCon-900S Operator’s Manual - If liquid crystal enters your eyes, flush the affected eye with clean water for at least 15 minutes and then seek medical assistance. - If liquid crystal is swallowed, rinse your mouth thoroughly with water. Drink large quantities of water and induce vomiting, then seek medical assistance.
CAUTION
Use the system indoors only. Do not use the system if it exhibits erratic or inconsistent behavior. Shut down the system and contact Mcube Technology or your local distributor. Do not spill liquid on the system.
2.6 COMPLIANCE STATEMENTS Federal Communication Commission Interference Statement This equipment has been tested and found to comply with the limits for a Class A digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference when the equipment is operated in a commercial environment. This equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the instruction manual, may cause harmful interference to radio communications. Operation of this equipment in a residential area is likely to cause harmful interference in which case the user will be required to correct the interference at his own expense.” This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) This device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.
FCC Radiation Exposure Statement: This equipment complied with FCC radiation exposure limits set forth for an uncontrolled environment. This equipment should be installed and operated with minimum distance 20cm between the radiator & your body.
CAUTION
Any changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate this equipment.
IC Statement This Class A digital apparatus complies with Canadian ICES-003. This device complies with Industry Canada license-exempt RSS standard(s). Operation is subject to the following two conditions: (1) this device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device. Cet appareil numérique de la classe A est conforme á la norme NMB-003 du Canada.
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CUBEScanTM BioCon-900S Operator’s Manual
2.7
SAFE HANDLING PROCEDURES FOR TRANSPORTER
Quarantine: Packages that are crushed, punctured or torn open to reveal contents should not be placed into deployment. Such packages should be isolated until the shipper has been contacted, provides disposition instructions and, if appropriate, arranges to have the product inspected and repacked. Spoiled Product: In the event that damage to packaging results in damage to the battery causing released electrolyte, the spill should be contained and the shipper should be contacted for instructions.
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CUBEScanTM BioCon-900S Operator’s Manual
3
INTRODUCTION
3.1
PRODUCT FEATURES
The main components of CUBEScanTM BioCon-900S are a Probe and the Charger.
BioCon-900S Probe & Charger Hand-held, portable and lightweight Touchscreen interface Measures bladder volume with ultrasound Provides a live image of bladder during Pre-scan Takes scans and provides scan results in a short time Easy to use: staff can easily learn how to scan patients in a short time Battery-operated, wireless charging
Figure 1 CUBEScanTM BioCon-900S
3.2 No.
SYSTEM COMPONENTS Picture
Parts
Q’ty
Description
1
BioCon-900S (Probe)
1
Hand-held, wireless, battery-operated, touchscreen, ultrasound probe
2
Charger
1
Use the Charger to charge BioCon900S’s internal battery.
3
Mobile Cart (MRC-900S)
1
Mobile cart (Optional Component)
4
AC/DC Adapter
1
Use only with the Charger.
5
Power cord
1
The type of power cord depends on your country.
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CUBEScanTM BioCon-900S Operator’s Manual
6
-
Barcode Module
1
Reading a barcode with information for a patient. (Optional Component)
7
-
Operator’s manual
1
-
Users can replace only gel The other parts are not allowed for the users to disassemble or replace except the gel. Please contact your local distributor or Mcube Technology. Only use the ultrasonic gel approved by FDA, CE.
OUTER APPEARANCE – PROBE
3.3
Figure 2 Probe Appearance No.
Part
Function
1
Touchscreen Display
Displays bladder volume and other information.
2
Power Button
Press to turn the probe on or off and release
3
Scan Button
Press to take a scan
4
Probe Head
5
Power Indicator
Generates, transmits and receives ultrasound waves, produces a 3D image of bladder. Type BF applied part Indicates power status. Orange solid – System is being booted Yellow solid – Power on status Off – Power off
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CUBEScanTM BioCon-900S Operator’s Manual
6
Battery indicator
Indicates charging status. Orange solid - Battery is being charged. Off – Battery is fully charged.
7
Barcode Module
Reads printed a barcode
8
Laser Safety Label
Explanatory label – Class 1 laser product
9
Label
Put on this label when there is no optional barcode module
10
Back Label
NOTE : Labels are subject to change without prior notice
NOTE: The appearance of these labels(No.8 - 9) depends on wheter the barcode option is selected or not.
OUTER APPEARANCE - CHARGER
3.4
Figure 3 Charger Front-View No.
Figure 4 Charger Bottom-View
Item
Function
1
Battery indicator
Indicates charging status. Green (Solid) – Power cord is connected or Charging is completed. Green (Blink) – Charging.in progress Yellow (Solid) – Error Status
2
Silicone pad
Anti-skid pad
3
Insert Nut
Insert nut to secure the Charger to the mobile cart (MRC-900S). It prevents movement or damage of Charger from shock.
4
Label
5
AC/DC Adapter Inlet
AC/DC adapter inlet
6
Vents
Ventilate the Charger.
NOTE : Labels are subject to change without prior notice
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CUBEScanTM BioCon-900S Operator’s Manual DISPLAY AND ICONS
3.5
A touch-screen display allows you to perform scans, manage results and setup. The Home screen appears when the probe is turned on. It services as a starting point for all the main functions of the device. You can select the desired icons by tapping them directly on the touch-screen.
No.
Description
1
Status – Current time, the number of saved data and battery status.
2
Main Display – controls the user interface
Figure 5 Home Screen
ICON DIRECTORY
3.6
Patient Type Icon
Description Male (All other patients) Female Patient – A female who has not had a hysterectomy Female Patient – A female who has had a hysterectomy Pediatric Patient – A child with height less than 47 inches (120cm) and weight less than 55 lbs(25kg).
Home screen Icon
Description Review – Go to the Review screen. Missing Data – Go to review the missing (unsaved) scan result. Setup – Go to the Setup screen. Battery status.
Information screen & Pre-scan screen
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CUBEScanTM BioCon-900S Operator’s Manual Icon
Description Barcode - Record a barcode (Optional) Home – Return to the Home screen. Scan – Perform the Normal scan or Pre-scan. Exit –Return to the Information screen.
Scan Result screen Icon
Description Aiming Information – Rotate 15° clockwise, indicating the aiming point of the bladder. Urine Volume – Measured urine volume.
P1
Plane No. – The 1st plane of 12 planes of the result (PX – The ordinal number of 12 planes) Scan – Re-scan the bladder. Home – Return to the Home screen. Save – Save the scan result.
Review screen Icon
Description Delete – On the Review screen, delete what is currently being displayed. OK – Select the option or perform the action. Cancel – Cancel the current function. Previous – On the Review screen, move to the previous patient scan result. Next – On the Review screen, move to the next patient scan result. Exit –Return to the Home screen.
Setup screen Icon
Description Date format (YY-MM-DD, DD-MM-YY,MM-DD-YY) Date Time (format : 24-hour)
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CUBEScanTM BioCon-900S Operator’s Manual Sleep mode (2min, 3min, 5min) Display brightness (0 to 100%, default= 50%))
Pre-scan On (
) / Off (
)
Delete all saved results. Calibration Reminder On (
) / Off (
)
Self-test (YY/MM/DD) Phantom Calibration (YY/MM/DD) CalKit Calibration (YY/MM/DD) On the self-test or calibration screen, perform self-test or calibration Cease – On the self-test or calibration screen, cease self-test or calibration Exit – Return from the self-test or calibration screen to the Setting screen. Previous – Move to previous page. Next – Move to next page. Home – Return to Home screen. OK – Select the option or perform the action. Cancel – Cancel the current function.
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CUBEScanTM BioCon-900S Operator’s Manual
4. SETUP See the section “4.1 ACCURACY OF MEASUREMENT” before use. Check the probe’s battery has sufficient power through battery icon. If the battery has not been
4.1
sufficiently charged, recharge the battery before bladder measurement. Wipe the probe head gently with a soft cloth dampened in cleaning and disinfection agents to clean and disinfect the probe. See the section “8.3 CLEANING & DISINFECTION”.
ACCURACY OF MEASUREMENT
Following cases affect ultrasound transmission and accuracy of measurement.
When a patient has had supra-pubic or pelvic surgery. A patient with catheter in his or her bladder. A patient with scar, sutures, staples or incisions in his or her abdomen. Use of unsuitable ultrasound gel . Air bubbles between probe head and the skin of the patient. An excessive obese patient. Use of the probe with an unclean probe head. Inappropriate patient position.
4.2
CHARGE THE BATTERY WARNING
The battery must be replaced by the authorized service provider only. Use only the provided Charger and power cord to charge the battery for electric safety. Do not disassemble, heat or incinerate the battery. Keep battery out of reach of children and in original sealed package. Dispose of used batteries promptly according to local recycling or waste regulations. To reduce the risk of leakage, explosion, fire, or serious injury, note the following when handling the
lithium-ion battery included in the system: - Never short-circuit the battery by either accidentally or intentionally bringing the battery terminals into contact with any other conductive objects. This could cause serious injury or fire and could also damage the battery and BioCon-900S. - Never expose the battery to abnormal shock, vibration or pressure. The battery’s internal protective covering could fail, causing it to overheat or ignite, resulting in caustic liquid leakage, explosion or fire. Avoid charging near fire or in the sunlight. Do not use the Charger for other equipment.
CAUTION
The Charger, power cord, and adapter are not intended for patient contact. Ensure 6 ft (2 m) are
maintained between the patient and these components. Immediately discontinue use of the battery, if the battery emits an unusual smell, feels hot, changes color or shape, or appears abnormal in any other way. Contact Mcube Technology or your local distributors.
The probe is powered by a internal lithium ion battery. The battery is charged by Charger and the Battery
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CUBEScanTM BioCon-900S Operator’s Manual Status icon ( ) is always displayed in the Status at the top of the screen, indicating the current capacity. Before using the probe for the first time, you must fully charge the battery. When you don’t use your probe, we recommend that you mount and store it on the Charger to ensure that the probe is sufficiently charged. The battery is protected by protection circuit module and have the functions of overcharge, overdischarge and overcurrent prevention to maintain safety and prevent significant deterioration of cell performances. To conserve battery life, the probe is configured to go into sleep mode. The probe goes into sleep mode when you press the Power Button( ) twice or if the probe has not been touched in the designated time with power on. You can adjust the time for sleep mode in the setup(2min/3min/5min), if necessary. See the section“7.4 SLEEP MODE SETTING”. Shortly press the Power Button(
Figure 6 Probe-mounting
Figure 7 Probe Indicatior
) to wake up the system.
Figure 8 Charger Indicator
1) Connect the AC/DC adapter to the power cord. 2) Connect the AC/DC adapter to the Charger 3) Plug the AC/DC adapter into an electric outlet 4) The battery indicator (3) on the Charger lights on in steady green (Power on). 5) Mount the probe on the Charger. Make sure that the upper part of probe reaches the wall of Charger. See Figure 5. 6) As soon as the probe is mounted on the Charger, the beep and light indicators work as below; a) A short beep: A connection for the probe’s battery charging is completed. b) The battery indicator (3) on the Charger lights on in blinking green(Charging in progress). c) The battery indicator (2) on the probe lights on in steady orange (Charging in progress). 7) The Power indicator (1) is turned on in steady yellow when the probe is ready to use. 8) It takes approximately 6 hours for the discharged battery to fully charge. When fully charged, the battery indicator(2) on the probe turns off.
4.3
SCAN TYPE
You can adjust one of the following options to measure bladder volume: Pre-scan: General 2D real-time ultrasound scanning. 2D ultrasound images are displayed continuously in live image basis. This helps an operator locate bladder position and predicting the range of residual urine to detect the bladder before normal scan. Normal Scan: Get 12-plane ultrasound images and calculate the residual urine in the bladder (3D scanning).
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CUBEScanTM BioCon-900S Operator’s Manual
5 HOW TO USE CHECKUP BEFORE USE
5.1
Before using BioCon-900S, ensure you are familiar with the device and its parts. If you use it for the first time, we strongly recommend you to try your first bladder volume measurement on a patient with moderately full bladder using Pre-scan. Pre-scan helps you detect the bladder and moderately full bladder can be located more easily.
WARNING
If you use BioCon-900S in the presence of flammable anesthetics, explosion hazard exists. Do not use the BioCon-900S on following cases: 1) Fetal use or pregnant patients. 2) Patients with ascites. 3) Patients with open or damaged skin. 4) Wounds in the suprapubic region.
CAUTION If the oil leaks from housing and fluid gets in contact with your eyes, skin or clothing, flush the affected area immediately with clean water and seek medical attention or see a doctor.
5.2
TURN SYSTEM ON/OFF
There are two power modes to system on/off the BioCon-900S. Loading screen depends on the power mode and it shows during start-up.
Figure 9 Loading Screen (1)
5.2.1
Figure 10 Loading Screen (2)
Figure 11 Home Screen
SLEEP MODE
To preserve battery power, the probe goes into sleep mode by shutting itself down automatically when not in use. You can set the time to go into sleep mode in the setup (2min/3min/5min). See the section “7.4 SLEEP MODE SETTING”. However, if a battery needs to be recharged immediately, Dialog box ( ) appears shortly and then probe goes to sleep mode by shutting itself down. We strongly recommend that you should recharge the battery immediately. See the section “4.2 CHARGE THE BATTERY”.
Turn System on
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