Contec Medical Systems BC401 User Manual
User Notice
1.Thanks for purchasing Urine Analyzer! Please read the User Manual
carefully before using this product. The User Manual which describes
the operating procedures should be followed strictly.
2.This manual detailed introduce the steps must be noted when using
the product, operation which may result in abnormal. Any anomalies
or personal injury and device damage arising from use, maintain, store
do not follow requirements of the User Manual, Our company is not
responsible for the safety, reliability and performance guarantees! The
manufacturer’s warranty service does not cover such faults!
3.The device with data storage function, for user losses which caused
by data loss due to device damage or user's operation, our company
does not assume any responsibility.
4.Test strip can only choose regular products, it's recommended to use
the test strip which supplied with the device, so better ensure the
accuracy of the test.
5.Our Company reserves the right to change the content of the manual,
the contents of this manual are subject to change without notice.
I
Statement
This user manual contains proprietary information, which is protected
by copyright. All rights reserved. Reproduction, adaption or
translation, for any part of the manual without prior written
permission, is prohibited.
Our company assumes no responsibility for incidental or
consequential damage in use caused by any error appear in this
document. In case of product upgrades, the information contained in
this manual is subject to change without notice.
Our company reserves the final elucidative right.
Meaning of symbol
Note : Tips, advice and suggestions.
Warning : Warnings must be complied strictly to ensure
that the Urine Analyzer can operation normally and the test result
are correct and true.
In vitro diagnostic medical equipment.
Equipment which all protected by double insulation or
reinforced insulation.
ISO7000-0659, Biohazard.
WEEE (2002/96/EC).
Refer to instruction manual/booklet.
Date of manufacture.
II
Serial number.
Manufacturer.
This item is compliant with In Vitro Diagnostic Medical
Device Directive 98/79/EC of Dec.27,1998, a directive of the
European Economic Community.
FCC WARNING
This device complies with part 15 of the FCC rules. Operation is subje
ct 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.
Changes or modifications not expressly approved by the party
responsible for compliance could void the user’s authority to operate
the equipment.
NOTE: This equipment has been tested and found to comply with the
limits for a Class B digital device, pursuant to part 15 of the FCC
Rules. These limits are designed to provide reasonable protection
against harmful interference in a residential installation. This
equipment generates uses and can radiate radio frequency energy and,
if not installed and used in accordance with the instructions, may
cause harmful interference to radio communications. However, there
is no guarantee that interference will not occur in a particular
installation. If this equipment does cause harmful interference to radio
or television reception, which can be determined by turning the
equipment off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
- Reorient or relocate the receiving antenna.
III
- Increase the separation between the equipment and receiver.
-Connect the equipment into an outlet on a circuit different from that
to which the receiver is connected.
-Consult the dealer or an experienced radio/TV technician for help
RF Exposure
When using the device, ensure that the antenna of the device is as least
20 cm away from all persons.
IV
Content
User Notice ................................................................................... I
Statement ..................................................................................... II
Content ........................................................................................ V
Chapter 1 Overview ...................................................................... 1
1.1 Summarization ................................................................ 1
1.2 Precautions for Use ......................................................... 2
1.3 Technical Specification................................................... 3
Chapter 2 Installation .................................................................... 5
2.1 Operation Environment .................................................. 5
2.2 Dismantlement and Installation ...................................... 5
2.3 Appearance and Structure ............................................... 6
2.3.1 Front View ........................................................... 6
2.3.2 Back View ........................................................... 7
2.4 Power Supply .................................................................. 7
Chapter 3 Operation ...................................................................... 9
3.1 Buttons ............................................................................ 9
3.2 Power On ...................................................................... 10
3.3 Start Test ....................................................................... 11
3.4 Power Off ..................................................................... 13
3.5 Setup Menu ................................................................... 14
3.5.1 Records .............................................................. 14
3.5.2 Unit .................................................................... 16
3.5.3 Clock .................................................................. 16
3.5.4 Language ............................................................ 17
3.5.5 Factory Settings ................................................. 17
3.6 Instructions of Bluetooth .............................................. 20
3.6.1 Scope of Application ......................................... 20
3.6.2 Operating Steps of Bluetooth Communication .. 21
3.6.3 Other Descriptions ............................................. 21
Chapter 4 Maintenance ............................................................... 22
4.1 Maintenance .................................................................. 22
4.2 Dismantle and Install the Paper Tray ............................ 22
V
4.3 Clean the Paper Tray .................................................... 23
4.4 Disinfection .................................................................. 24
4.5 Waste Disposal ............................................................. 24
4.6 Troubleshooting ............................................................ 24
Appendix .................................................................................... 26
VI
Chapter 1 Overview
1.1 Summarization
Urine test is the most common method for checking disease in clinical
test, and checking with urine test strip is the most effective method.
urine test strip and urine sample produce a chemical reaction, the color
of each test color-area will change after reaction, the corresponding
test results can be obtained according to the color change. The
analyzer is researched and developed basing on modern photoelectric
and microprocessor technology for clinical inspection of urine, and it
integrates the advantages of easy and quick operation, exact result.
Features:
High-luminance and white LED, improves Signal Noise Ratio;
High-performance photoelectric receiving components, RGB
tricolor test theory, which makes the analyzer possess the
function of good anti-interference and adaptability;
User-friendly interface, features in vivid arrangement and
convenient use;
With flash memory technology, automatic synchronization
storage during testing process, and the data doesn't lose when the
device power off or unexpected shut down;
Store up to 500 test results, manage according to date and sample
NO, which is convenient for consulting;
Compatible with 8 items, 10 items and 11 items of test paper;
With a rechargeable battery that can be tested anytime, anywhere.
Purpose:
Use with the dedicated urine test strips for clinical urine testing.
Life:
Under the conditions of daily maintenance, normal use time is
not less than five years.
1
1.2 Precautions for Use
Note
Before using, please read the Manual carefully and strictly
operate according to it.
Please don't use the accessories not provided by manufacture.
Please don't use the analyzer in condition that the test strip is
expired or the device is damaged.
Please transport, install and operate the analyzer following the
User Manual.
To ensure the accuracy, the operation temperature should be in
range of 10℃-30 , if exceeds this range, place ℃ the analyzer in
required environment for 20-30 minutes before using.
Away from the strong electric field (magnetic field) when using,
avoid direct sunlight.
Use the supporting test strip which specified by the manufacturer.
2
1.3 Technical Specification
Glucose(GLU), Bilirubin(BIL), Specific
gravity (SG), PH, Ketone body(KET), Occult
Test item
Test mode Single-step test
Language Chinese and English
Display LCD, resolution:320*240
Principle RGB tricolor test theory
blood(BLD), Protein(PRO),
Urobilinogen(URO), Nitrite(NIT),
Leukocytes(LEU), Ascorbic acid (VC)
Communicatio
n interface
Mini USB interface, Bluetooth wireless
communication(apply to BC401BT)
Repeatability CV≤1%
Stability CV≤1%
Record mode LCD display, FlashROM data storage
Relative
≤80%
humidity
Built-in rechargeable lithium battery 3.7V,
1900mAh
Power supply
Host computer: DC 5V, 1A
Adapter: AC 100V-240V, 50/60Hz
Test r ange Refer to Grads Table in appendix
Input power
≤5W
consumption
Temperature: 10 ~30℃℃
Relative humidity: ≤80%
Operating
environment
Atmospheric pressure: 76kPa~106kPa
Away from the strong electric field (magnetic
field), avoid direct sunlight
3
Dimension 126mm(L)*73.5mm(W)*30mm(H)
4
Loading...