Omron Colin VP-1000 plus, Colin BP-203RPE III User Manual

Thank you for purchasing the OMRON BP-203RPE3 unit.

Read all of the instructions in the manual before you operate the unit and keep the manual near the unit at all times for future reference.

Non-invasive Vascular Screening Device

BP-203RPE

Contents

1. Before Use

1-1. Exemptions .................................................................................................. 3

1-2. Intended Use................................................................................................ 4

1-3. Meaning of Symbols ................................................................................... 5

1-4. Safety Information....................................................................................... 6

Explanation of Symbols........................................................................... 6

1-5. Product and Accessories .........................................................................13

Main Unit ............................................................................................... 13

Standard Accessories............................................................................ 13

Accessories (Sold Separately) .............................................................. 15

Options .................................................................................................. 16

1-6. Name and Function of Each Part .............................................................17

Main Unit ............................................................................................... 17

Stand ..................................................................................................... 18

1-7. Installation/Moving .................................................................................... 19

Inspection Before Starting Work ............................................................ 19

Procedure for Moving ............................................................................ 20

2. Measurement Procedure

2-1. Preparing for Measurement ...................................................................... 22

Measurement Procedure .......................................................................22

Patient Information ................................................................................ 23

Initial Screen (ID Entry Screen) ............................................................. 24

Entering and Editing Patient Information............................................... 25

Displaying the Measurement History..................................................... 40

Attaching the Cuff and Sensor............................................................... 41

2-2. Basic Measurement................................................................................... 47

Viewing the Measurement Screen......................................................... 47

Contents of the Measurement Screen................................................... 48

Starting and Ending Measurement ........................................................ 51

2-3. Measurement Results ............................................................................... 53

Contents of the Measurement Results Screen...................................... 53

Measurement Results Reports .............................................................. 54

2-4. R-R Interval Examination ..........................................................................65

Starting and Ending R-R Interval Examination ...................................... 65

R-R Interval Examination Results.......................................................... 66

2-5. Stress Mode ............................................................................................... 67

Starting and Ending Stress Test............................................................. 67

Checking Numerical Values During Stress Test .................................... 71

Stress Test Results................................................................................ 73

3. Settings and Data Processing

3-1. Main Menu Screen..................................................................................... 74

3-2. User Default Settings ................................................................................76

Items That Can Be Set ..........................................................................76

User Default Settings Procedure ........................................................... 79

3-3. Print Default Settings................................................................................ 80

Items That Can Be Set .......................................................................... 80

Print Default Settings Procedure ........................................................... 85

3-4. Facility name / Doctor / Technician / Category Settings......................... 86

Selecting the List Entry Method............................................................. 86

List Entry Procedure .............................................................................. 87

Pre-selection Setting Procedure............................................................ 91

3-5. Date & Time Settings................................................................................. 93

3-6. Printing Reports and Editing Patient Information.................................. 94

Reprinting Measurement Data............................................................... 95

Editing Patient Information .................................................................... 97

Deleting Measurement Data.................................................................. 99

3-7. Printing a Trend Report .......................................................................... 101

3-8. Advanced Registration of Patient Information ..................................... 105

Selecting the Registration Method....................................................... 105

Registration Procedure........................................................................ 106

Editing Patient Information .................................................................. 109

Deleting Patient Information ................................................................. 111

3-9. Printing Usage Frequency / Facility Patient Reports ........................... 113

Types of Reports ................................................................................. 113

Procedure for Printing Usage Frequency /

Facility Patient Reports......................................................................... 115

3-10. Data Export / Import (USB Flash Drive)................................................. 116

Data Processing Items ......................................................................... 116

Data Processing Procedure................................................................. 117

3-11. Transferring Report Data (PC)................................................................ 120

4. Options

4-1. Options .....................................................................................................121

TBI package ........................................................................................ 121

HMC package...................................................................................... 122

Bar Code Reader Set ..........................................................................123

5. Maintenance

5-1. Routine Maintenance .............................................................................. 124

Maintenance Procedures......................................................................124

Supplies................................................................................................125

5-2. Replacing Cuffs .......................................................................................126

Replacing an Arm Cuff ........................................................................ 126

Replacing an Ankle Cuff ...................................................................... 126

5-3. Connections............................................................................................. 127

Connectors on the Device ................................................................... 127

Basic Connections................................................................................128

5-4. Changing the Arm Position ..................................................................... 129

5-5. Handling Errors ........................................................................................132

Types of Audible Alarms....................................................................... 132

5-6. Displaying System Information............................................................... 133

5-7. Maintenance Menu ................................................................................... 134

5-8. Specifications ...........................................................................................135

5-9. Guidance and Manufacturer's Declaration ............................................139

5-10. Explanation of Technical Terms.............................................................. 143

5-11. Disposal .................................................................................................... 147

1. Before Use

1-1. Exemptions

Disclaimer

Principles

Trademark

Our company assumes no responsibility for the following:

1.Failures, damage, or injuries due to maintenance or repair work performed by other than our company or a company that we specify.

2.Failures or damage to one of our products caused by a product of another manufacturer not delivered by us.

3.Failures, damage, or injuries due to maintenance or repair work using a repair part other than a part that we specify.

4.Failures, damage, or injuries caused by failure to observe the safety instructions and operational procedures given in this manual.

5.Use of the product in conditions that do not conform to the product usage conditions indicated in this manual, including power, installation, and storage conditions.

6.Failures, damage, or injuries due to modification or inappropriate repair of the product.

7.Failures, damage, or injuries due to natural calamities such as fire, earthquake, flooding, or lightning.

1.The contents of this manual are subject to change without notice.

2.Considerable care has been taken in the preparation of this manual. In the unlikely event that an error or other problem is discovered in the manual, please contact us.

3.Unauthorized reproduction of all or part of this manual is prohibited. Use other than individual (corporate) use without the permission of our company is prohibited by copyright.

Product brand names shown in this manual are likely to be the trademark or registered trademark of the company concerned.

1-2. Intended Use

Medical Purpose

This is a non-invasive diagnostic system designed to assist in the detection of peripheral vascular diseases.

Using Population

Legally certified medical experts, such as doctor, nurse and ME.

Patient Population

It is used on adult patients only.

Environment

The instrument is used in a vascular laboratory, clinic, hospital, doctor's office, and other medical facilities where the non-invasive peripheral vascular test is conducted.

Durable Period

5 years, provided that the appropriate maintenance has been done from production date.

(Self-certification through OMRON HEALTHCARE's own data)

Measurement Parameter

■ Non-invasive Blood Pressure

■ Heart Rate

■ Pulse Wave

■ Heart Sound

Calculating Parameter

■ ABI (Ankle Brachial Index)

■ Pulse Wave Velocity

■ Augmentation Index

■ Systolic Time Interval

■ Upstroke Time

Precautions for use

Warnings and cautions described in the instruction manual should be observed.

1-3. Meaning of Symbols

Start (of action) This way up

Stop (of action) Keep away from rain

Caution (Refer to safety information)

Stacking limit by number

Consult instructions for use Temperature limitation

Authorised representative in the European community

Catalogue number

Manufacturer Disposal instructions

Date of manufacture Use by

Do not reuse Batch code

Defibrillation-proof type BF applied part

Fragile; Handle with care

Defibrillation-proof type CF applied part

Gruene Punkt (Green point in German)

CE mark Serial number

1-4. Safety Information

The warning signs and symbol examples indicated below are intended to ensure safe use of the product and prevent damage and injury to you and others. The signs and symbols are explained below.

Explanation of Symbols

* Physical damage means serious damage to your house and household goods, and serious injury

to pets or other domestic animals.

Warning

Indicates a situation where incorrect handling may cause human death or serious injury.

Caution

Indicates a situation where incorrect handling may cause human injury or physical damage.*

indicates "mandatory" (an action that must be observed).

The actual action that is mandatory is indicated inside or next to . The icon at left indicates "disconnect the power plug".

indicates "forbidden" (an action that must not be taken).

The actual action that is forbidden is indicated inside or next to

The icon at left indicates that "disassembly is forbidden".

Note:

This indicates information that should be known when operating the device.

1-4. Safety Information

Warning:

Safety rules when using the product

Do not use a frayed or damaged power cord or plug. Otherwise electric shock, short circuiting, or fire may result.

Do not touch the power plug with wet hands. Otherwise electric shock or injury may result.

Be sure to plug the three-prong power plug into a grounded (three-prong) outlet for medical use (when a printer is included). Otherwise electric shock or current leakage may result.

Use a dedicated outlet. Otherwise electric shock or current leakage may result.

Do not poke or scratch the buttons or display with a sharp or pointed object. Incorrect diagnosis and treatment or an accident may result.

Do not connect the power plug to the outlet if the electrical ratings are outside the specified range below: 100 - 240 VAC. This may cause fire.

Do not touch the unit when discharging a defibrillator.

Safety rules when performing measurement

This device is only to be used by qualified medical personnel, or under the guidance of such personnel. Otherwise incorrect diagnosis and treatment or device failure may result.

The results of measurement should only be interpreted by a doctor. If you are concerned about a measurement result, consult your doctor. Otherwise incorrect diagnosis and treatment may result.

This device is intended to perform measurement for examination. Do not use the device for patient monitoring. Otherwise an accident may result.

If pressurization does not stop during measurement or another abnormal condition occurs, remove the cuff or air tube and disconnect the power. Otherwise peripheral nerve may be damaged.

Use only the specified supplies for the cord, cuff, USB devices, and other parts. Do not install other than specified options. Otherwise an accident may result.

Do not connect the air tube or cuff to any other device tubes attached to the body. Otherwise air may enter the blood vessels and an accident may result.

1-4. Safety Information

Do not attach the arm cuff for patient during medical treatment with intravenous drip or blood transfusion. This may result incorrect diagnosis and treatment.

Do not use this device on a patient that cannot express pain. If cuff pressurization does not stop in a specified time, internal hemorrhaging may occur in the upper arm or ankle.

This device cannot be used during MRI imaging. This may cause an accident.

Pay constant attention to patient's condition during measurement. Otherwise an accident may result.

Do not perform measurement without cleaning and sterilizing the device, cuffs and sensors after measuring for patient with infection.

Pay extra attention to a patient with pacemaker during measurement. Rate meters may continue to count the pacemaker rate during occurrence of cardiac arrest or some arrhythmias. Do not rely entirely upon rate meter alarm. Refer to the pacemaker pulse rejection capability in this manual.

Installation

As this device conforms to the IEC60601-1-2 standard, it can be used in combination with another medical device. While or after an electrosurgical knife or a device which generates noise being used near this device however, make sure that it is properly functioning. Otherwise incorrect diagnosis and treatment or device failure may result.

Do not use this device in the presence of a flammable gas such as a highly inflammable anesthetic, or in a high-pressure oxygen chamber or tent. Fire and explosion may result.

Do not install or store the device in a location where water or chemicals may splash on the device. Electric shock may result.

Do not connect any electric device, without the approval of IEC60601-1, or not fulfilling IEC60601-1-1. For the use of a PC or a printer with this device, the connecting device should be approved according to standards mentioned above. (This unit meets the restricted level of leakage current required for medical devices and it does not include all the connected devices. Connecting to other device is not allowed unless the total leakage current of such a combination is within the restricted level.) Neglecting this caution, it could cause electric shock to the device.

Maintenance

After cleaning the device, dry it completely before turning on the power again. Otherwise electric shock or current leakage may result.

1-4. Safety Information

Caution:

Safety rules when using the product

Observe the rules below when handling the power cord. Failure to observe these rules may result in electric shock or device failure.

•Do not damage the cord

•Do not break the cord

•Do not modify the cord

•Do not bend or pull on the cord with undue force

•Do not twist the cord

•Do not tightly coil the cord when in use

•Do not place heavy objects on the cord

•Do not let the cord become pinched

Insert the power plug all the way into the outlet. Otherwise electric shock, short circuiting, or fire may result.

Wipe dust off the power plug. Otherwise electric shock, short circuiting, or fire may result.

After using the device, turn the power switch to the "off" position and disconnect the power plug. Failure to do so may cause deterioration of the insulation and result in electric shock, current leakage, or fire.

When removing the power plug from the outlet, grasp and pull on the plug, not the cord. Pulling on the cord may break wires and cause a short circuit, resulting in fire or electric shock.

If a power failure occurs while using the device, turn the power switch to the "off" position and disconnect the power plug. Failure to do so may result in a product failure or other problem.

If the device becomes wet, wipe it completely dry with a soft cloth before use. Otherwise electric shock, short circuiting, or fire may result.

Safety rules when performing measurement

If the patient has any of conditions below, do not perform measurement. Otherwise incorrect diagnosis and treatment may result.

•The patient has an aneurysm

•The patient has insufficient peripheral circulation, noticeably low blood pressure, or low body temperature.

•The patient frequently has an irregular pulse.

In the following situations, check by auscultation or palpation. Otherwise incorrect diagnosis and treatment may result.

•When irregular pulse waves are indicated. External vibration or patient movement during measurement may cause an incorrect indication.

•When an error occurs or when a measured value is questionable.

1-4. Safety Information

If a power failure occurs during measurement, immediately remove the cuff. If the patient's ankle or upper arm is pressurized for a long time, internal hemorrhaging may result.

Do not attach the cuff on the measurement site below:

•Arm with intravenous drip

•Upper limb in which a shunt is placed in for hemodialysis Incorrect diagnosis and treatment or an accident may result.

If there is acute inflammation, a pyogenic ailment, or an external wound where the cuff is to be attached, follow the instructions of a doctor. Symptoms may become worse.

When there is impossibility of test or doubts about the measurement values, please confirm the patient's condition first. The patient's condition may have deteriorated to the point where measurement limits are exceeded. Always verify that the cuff and cuff hose are appropriately used and are not bent or blocked. If the display continues to show 0, the monitor's pressure may be 0. But if the cuff hose is blocked or bent there may be air remaining in the cuff. At this time disconnect the hose from the cuff to ensure that blood flow is not restricted and no disorders occur to the peripheral nerves.

When using the device in combination with another medical device, read the manual of the other device well and understand all warnings and cautions. Incorrect diagnosis and treatment may result.

Do not use the device in a location with loud noise. Incorrect diagnosis and treatment may result.

Attach the PCG sensor correctly. Incorrect diagnosis and treatment may result.

Take care that the PCG sensor does not fall on the patient. This may cause injury.

Wrap the cuff on bare skin or on a thin layer of clothing. Otherwise internal hemorrhaging may result.

Make sure that the ECG clips are attached in the correct positions. Otherwise incorrect diagnosis and treatment may result.

Do not use the device near a cellular phone. Incorrect diagnosis and treatment may result.

Do not use in an MRI, CT, X-ray room, an operating room, or other rooms where radio noise is generated. Incorrect diagnosis and treatment or an accident may result.

Do not use a worn or expired ECG clip electrode or PCG sensor pad. Otherwise incorrect diagnosis and treatment may result. (ECG clip electrode and PCG sensor pad have an expiry date. After the expiry date, the pad becomes dry and incapable of accurate measurement. Use only a pad or electrode whose indicated expiry date has not passed. Refer to page 12 for how to confirm the expiry date.)

1-4. Safety Information

On a bedridden patient, check for lower-limb deep venous thrombus before taking a measurement. Otherwise an accident may result.

The ECG clip electrode and PCG sensor pad are disposable supplies. Do not reuse them once they are removed. In case that they are used on moist, injured or infected skin, dispose them right away. Otherwise an infection may result.

The sensor box removal lever uses a strong spring mechanism. Take care not to injure yourself on the metal edges. Hold the sensor box firmly and press down hard on the lever from the exterior to remove the connector. This may cause injury with the metal edges.

Do not use an air hose of an arm cuff or an ankle cuff that is bent or collapsed. Incorrect diagnosis and treatment may result.

Installation

Do not install in a location where the temperature or humidity is outside the allowed range. This may cause malfunctioning or device failure.

Do not use in a moving vehicle such as an ambulance. Incorrect measurement may result. Incorrect diagnosis and treatment or an accident may result.

If you are not using the device stand, exercise sufficient caution when moving the device. The device is heavy and may slip out of your hands, causing injury.

Do not place objects on the device. This may cause injury.

Maintenance

Do not disassemble, repair or modify the device. This may cause electric shock.

Before cleaning or maintaining the device, disconnect the power plug. Otherwise electric shock or injury may result.

1-4. Safety Information

Important:

Before use

• Make sure that all cords and tubes are firmly connected.

• Inspect dials and buttons and verify that the device operates correctly.

• Check printer toner, paper, and other supplies.

• Confirm the expiry date of the ECG clip electrode or the PCG sensor pad. The expiry date can be calculated from the lot number as follows:

During use

• Do not pressurize when the cuff is not wrapped.

• Do not use a torn cuff.

• The device may be used on the patients below. If used on patients other than those described below, incorrect measurement may result or measurement may not be possible.

- Height: 120 to 210 cm

- Girth of arm: 20 to 32 cm (using the standard cuff) / 16 to 38 cm (using the optional cuff)

- Girth of ankle: 16 to 33 cm

• Do not disconnect the USB or LAN cable while data is being transmitted. This may corrupt the data.

• Do not turn off the power during printing, data transmission, or writing.

• Do not pull out the paper before printing is finished.

• Make sure the date and time setting is correct. If the date and time setting is not correct, the date and time of measurement will not be recorded correctly.

• Do not connect an ECG clip to another conductive part including the ground.

• The electrical energy from a defibrillator may damage the device. During defibrillation, remove the sensors from the patient and do not touch the device.

• When moving or using the device, do not drop or subject the device to shock. This may cause the electric components and precision mechanisms to fail.

After use

• Clean the device and accessories and arrange properly for storage.

• Do not wash or moisten the cuff

• Do not use solvents such as thinner, benzene, or concentrated alcohol to clean the device

• Do not use an autoclave, ultraviolet radiation, or gas disinfection (EOG, formaldehyde gas, concentrated ozone, etc.) to disinfect the device

• If a fuse blows, there may be a problem in the device. Contact a dealer or an Omron Healthcare technical support representative

• Do not install the unit in the following locations

- A location with prolonged exposure to direct sunlight

- A location with dusty or salt air

- On an inclined surface or a location subject to vibration, shock, or noise

- A location where chemicals are stored or gas is emitted

• If the patient has one of the following conditions, a correct measurement may not be obtained

- The patient has body movements due to convulsions caused by rheumatism or otherwise

- The patient has diabetic arteriosclerosis (blood pressure at leg joints tends to be high)

- The patient has false high blood pressure

- The patient has convulsions or tremors

• When the unit is incapable of ECG measurement, the message "Electrode removed" is displayed.

Lot Number:

Production Date: 2006 July 10th

Expiry Date: 2008 July

6071011

(2 years after the production date)

(Example)

1-5. Product and Accessories

Before using this product, make sure that no accessories are missing and that neither the unit nor the accessories are damaged. Contact a dealer or an Omron Healthcare technical support representative If any accessory is missing or damaged.

Main Unit

Non-invasive Vascular Screening Device BP-203RPE3

Standard Accessories

BP-203RPE3 stand

BP-203RPE3 stand cover

BP-203RPE3 hook-and-loop fastener for the sensor box

Power cord for main unit (0.8 m)

Power cord for printer (1.1 m)

BP-203RPE3 power tap

USB cable (for printer)

Items on this page will be assembled on delivery as follows:

1-5. Product and Accessories

BP-203RPE3 arm cuffs, left and right pair (M size: For arm girths from 20 to 32 cm)

BP-203RPE3 arm cuff hoses, left and right pair

BP-203RPE3 ankle cuffs, left and right pair

Sensor box

ECG clips

Phonocardiogram sensor (PCG sensor)

PCG weight

Sensor gel packet (consumable packet) 5 sets

• PCG sensor pad, 1 piece x 5

• ECG clip electrodes, 3 pieces x 5

Blood vessel model

BP-203RPE3 touch pen

BP-203RPE3 manual

Quick manuals

1-5. Product and Accessories

Accessories (Sold Separately)

Product description REF Model

Right arm cuff, S size 9999492-9 HEM-CS30-RIGHT

Right arm cuff, M size 9999490-2 HEM-CR30-RIGHT

Right arm cuff, L size 9999496-1 HEM-CL30-RIGHT

Left arm cuff, S size 9999494-5 HEM-CS30-LEFT

Left arm cuff, M size 9999491-0 HEM-CR30-LEFT

Left arm cuff, L size 9999498-8 HEM-CL30-LEFT

Arm cuff air tube (right) 9999505-4 HEM-CR30R-TUBE

Arm cuff air tube (left) 9999504-6 HEM-CR30L-TUBE

Ankle cuff (right) 9999500-3 HEM-CR31-RIGHT

Ankle cuff (left) 9999501-1 HEM-CR31-LEFT

ECG clips 9999503-8 HFA-RPE3-ECG

PCG sensor 9999507-0 HFA-RPE3-PCG

PCG weight 9999506-2 HFA-RPE3-W700

Sensor gel packet (20 sets) 9967933-0 HBP-FORM-101S

Blood vessel model 9999510-0 HFA-FORM-ARTVS

Touch pen 9996749-2 HBP-PEN

LAN cable (for hub use) 9997621-1 HFA-RPE3-LANS

LAN cable 9997622-0 HFA-RPE3-LANX

Toe standard disposable cuff 9957110-6 HBP-DCUFF-TBI31

Toe small disposable cuff 9957111-4 HBP-DCUFF-TBI32

Toe cuff tube (right) 9957112-2 HBP-FORM-TBICR

Toe cuff tube (left) 9957113-0 HBP-FORM-TBICL

Table-tap 9515310-5 HBP-RPE3-TAKO

Stand cover 9511950-0 HFA-RPE3-CVR

Hook-and-loop fastener for the sensor box 9511951-9 HFA-RPE3-SBF

1-5. Product and Accessories

Options

Software and unit options can be purchased to expand the functionality of the product. For details on the uses and functions of the options, see Chapter 4.Refer to "4-1. Options" (page 121)

TBI package

HMC package

BP-203RPE3 bar code reader set

• Bar code reader

• Attachment fittings

Product description REF Model

TBI package 9512233-1 HFA-TBI-ENG

HMC package 9512232-3 HFA-RPE3-HMCPE

USB cable for HMC package 9903144-6 HBP-RPE3-USB

Serial cable for HMC package 9903143-8 HBP-RPE3-SER

Bar Code Reader Set 9996743-3 HBP-RPE3-BAR

TBI package manual 9512236-6 HFA-RPE3-TBIME

HMC package manual 9512235-8 HFA-RPE3-HMCME

Affix S/N label

BP-203RPE3 Unit Serial Number

Product Package Classification

HMC Package

OMRON HEALTHCARE CO., LTD.

Non-invasive Vascular Screening Device BP-203RPE 3

Product Package License Certificate

This certificate is a registration certificate for the product package that you purchased, and certifies that you, the customer, have lawfully received a license from OMRON HEALTHCARE Co., Ltd. OMRON HEALTHCARE Co., Ltd. permits the customer to install and use this product package on the BP-203RPE 3 unit indicated in this license certificate.

1-6. Name and Function of Each Part

Main Unit

Enter patient information, configure settings, and perform measurement.

Top Back

1. LCD display (touch panel)

When configuring settings: Setting buttons appear. Touch the setting buttons with the touch pen to enter settings. During measurement: Measured values, measured waveforms, and operation buttons appear.

2. Jog dial

Settings can be entered using the jog dial. Turn the jog dial right or left to select an item and press to enter.

3. Display lamps

Off: Power is off Green (on): Power is on (normal mode) Orange (on): Power is on (sleep mode)

4. [START] button

Press to begin measurement.

5. [STOP] button

Press to interrupt and stop measurement. On the screen with the [BACK] button, the [STOP] button can be also used to return to the previous screen.

6. Brightness button

: This enables the "-" and "+" brightness buttons. : This darkens the screen. : This makes the screen brighter.

7. Power on/off switch

Turns the power on and off. The power is normally turned on and off with the power switch on the stand, so keep the main unit power switched on.

8. Connectors

For details on the connectors, see Chapter 5. Refer to "5-3. Connections" (page 127)

1-6. Name and Function of Each Part

Stand

1. Arm

The sensors are placed on this arm.

2. PCG sensor pocket

Stores the PCG sensor.

3. Main unit holder

The main unit is placed on this holder.

4. Casters

During examination, lock the casters to keep the stand from moving. Unlock before moving the stand.

5. Cable cover

This prevents dust from collecting on the connectors on the back of the main unit.

6. Arm stand / touch pen stand

Attach the arm either on the left or the right. Insert the touch pen stand on the side that is empty.

Refer to "5-4. Changing the Arm Position" (page 129).

7. Drawer

Store printing paper and other supplies in the drawer.

8. Cable hook

Hang the sensor box cable on this hook.

9. Tray

Stores supplies on the tray.

10.Laser printer holder

11.Cuff storage pocket

Store arm and ankle cuffs.

12.Handle

Hold this when moving the main unit.

13.Power on/off switch

Turns the power of the main unit, printer, and options on/off at the same time.

( ) position is to turn on the power. ( ) position is to turn off the power.

14.Back pocket

Stores manuals and the power cord (when moving the stand).

1-7. Installation/Moving

Inspection Before Starting Work

For safe and proper use, inspect the device at the start of each day. When installing the device, be sure to follow the instructions on pages 7 to 12.

Before turning the power on

Main Unit

• Is the sensor that directly touches the patient clean?

• Are the cords arranged properly?

• Is the device kept dry?

• Is there no damage on the device?

• Are the casters not broken or caught by any foreign object?

Power Cord

• Is the power cord placed safe from people stepping on?

• Are the power cords not damaged? Is power-line not exposed? Is the power cords not frayed?

Supplies

• Are ECG clip electrodes and PCG sensor pads ready?

• Does the printer have enough toner and paper?

• Is paper loaded in the printer?

After turning the power on

Main Unit

• No smoke or abnormal smell?

• No abnormal noises?

Check the date and time setting

• Are the date and time correct? If not, see page 93 to set the correct date and time.

Warning

Do not install or store the device in a location where water or chemicals may splash on the device. Electric shock may result.

Caution

Do not install in a location where the temperature or humidity is outside the allowed range. This may cause malfunctioning or device failure.

1-7. Installation/Moving

Procedure for Moving

When you need to move the device, follow the procedure below.

1. Turn the power switch to the off ( ) position.

2. Remove the power plug from the outlet and coil the

cord.

Please do not pull the power cord.

3. Store the sensors on the arm.

4. Store the cuffs in the cuff storage pocket.

5. Hang the sensor box cable on the cable hook.

1-7. Installation/Moving

6. Unlock the casters.

7. Grasp the handle and move the device.

Do not push or pull any other parts rather than the handle.

8. After moving the device, lock the casters to secure

the stand.

2. Measurement Procedure

2-1. Preparing for Measurement

Measurement Procedure

Turn the power on

Enter or check patient information

Attach the cuffs and sensors to the patient

Make sure that "ECG: OK" and

"PCG: OK" appear on the display

Press the [START] button

Measurement starts

To stop measurement, press the [STOP] button

Measurement ends.

Measurement results will be displayed and/or

measurement report will be printed.

Have the patient in a supine position on

the bed and remain quite

2-1. Preparing for Measurement

Patient Information

Patient information is required to properly maintain a measurement history. Input items marked "Required" must be entered.

*Entry is only required if it will be used with the initial screen set to order

number entry. Patient information must be stored in advance.

There are two methods for entering patient information. A Enter the patient's information on the touch panel at the time of measurement. B Enter the patient's information in advance from "Advanced Registration of Patient Information".

This is convenient for group examinations. Refer to "3-8. Advanced Registration of Patient Information" (page 105).

Item name Input Page

Required

Sex

Birth Date

Height

Name

Optional

Weight

Waist

Disease

Order Number*

Measurement Sensors

Measurement Sites

Upper limit of pressurizing

Synchro measurement

Doctor

Technician

Omron Colin VP-1000 plus, Colin BP-203RPE III User Manual

Specifications and Main Features

Frequently Asked Questions

User Manual