2022
Wondfo® FinecareTM FIA Meter III Plus
Int. Technical Suppor t Team
Presenter： Time：
01 Instrument overview
CONTENTS
02 Operation introduction
01 Instrument overview
Detection System of Finecare
Finecare FIA Meter (FS-112) Finecare FIA Meter Plus (FS-113)
Finecare FIA Meter III Plus (FS-205) Finecare FIA Meter Plus SE (FS-114)
Instruments Reagents Quality Controls
Basic Parameter
Name Finecare FIA Meter III Plus
Model num. FS-205
Sample type Whole blood, serum, plasma or urine
Methodology Immunofluorescence
Speed 20 test channels, 200T/h
System Linux
10 inch colorful touch screen
Operation mode
virtual keyboard
Language Chinese, English
20000 results storage
Memory
Intelligent results management
Printing Built-in thermal printer, HP external printer
Temperature control Yes
Cooling System Fan cooling
Transmission of internet &
Yes
serial port
Size （374×396×480.5）mm
Weight About 19.5 KG
Finecare Plus VS Finecare Ⅲ Plus
Appearance
Name Finecare II Finecare Plus Finecare Ⅲ Plus
Mode FS-112 FS-113 FS-205
Channels 1 1 20
Testing Speed 100T/h 100T/h 200T/h
Items 32 53 53
Temperature Temperature can be Temperature can be controlled
without
Control controlled around 25 ℃ around 25 ℃
Heat Dissipation without fan heatsink Fan cooling
Quality Control without with with
Displayer small touch screen 8-inch color touchscreen 10-inch color touchscreen
Printer thermal printer thermal printer thermal printer & external printers
Compare
Finecare Plus • Single channel, testing multiple items
• Compact, portable
• Super-large touchscreen
• Two detection mode
Suitable for clinics, health centers, small and medium-sized hospitals,
ambulance, ICU, ER, class C and D hospitals with small sample volume
• 20 channels, testing multiple items
Finecare Ⅲ Plus
• Self-clocking, automatic detection
• One sample can test several items, need enter patient information
only once, the result will print in the same paper.
• High speed of detection
Large and medium-sized hospitals, clinical centers, clinical laboratory,
ER, class A, B and C hospitals with large sample volume
Configuration
Touch Screen
Test Device Exit
ID Chip Port
Test Device Holder
Card Tray
Thermal Printer
Configuration
Vent
Instrument Port Area
Power Switch &
Power Connection
Configuration
Serial Port USB Interface
VGA Port Ethernet Port
Finecare Reagents
Test Name
Insert Sample Well Reaction Window
Direction
Bar Code Handle Buffer ID Chip
Finecare Reagents
Convenient Rapid Test Speed
Room temperature storage Get the result in 3-15 min
Simple Long shelf life
Simple procedure 24M
Principle of Finecare System
Fluorescence
Immunoassay
Principle of Finecare System
Photoelectric Converter
LED Excitation Light Source
Antigen
Fluorescent Labeled
Antibody
Capture Antibody
Sample Well Test Line Control Line
Finecare Reagents
Complete Test Menu
Diabetic & Fertility&Thyroi Cardiac Tumor Coagulation &
Renal Injury d Function
Markers Markers Inflammation COVID-19 Others
Markers Markers
5 items 13 items 11 items 4 items 7 items 5 items 8 items
HbA1c β-HCG T3 NT-proBNP AFP D-Dimer 2019-nCoV Antibody Vitamin D
MAU LH T4 BNP PSA D-Dimer(one step) 2019-nCoV IgM Cortisol
Cys C FSH TSH cTnI CEA PCT 2019-nCoV IgG S100β
NGAL Prog fT4 Myo fPSA CRP 2019-nCoV IgM/IgG Ferritin
β2-MG PRL fT3 CK-MB PCT/CRP 2019-nCoV Antigen Dengue NS1 Ag
E2 H-FABP SAA ASO
Testosterone cTnl/NT-proBNP IL-6 Total IgE
AMH cTnl/CK-MB/Myo iFOB
hsCRP
cTnT(one step)
Total 53 items
Lp-PLA2
Application Scenarios
ICU/CCU GP office Medium/Small lab
Emergency
Room Hospital lab Clinics
02 Operation Introduction
Test Procedure
1 Preparation
2 Software operation
3 Add sample on the reagent card
4 Test and get the result
Test Procedure
1. Put the instrument on a level, dry surface, away from direct sunlight. Connect the instrument with
provided power adapter, switch on the instrument.
2. The instrument will boot up, load on the system and enter the Login interface.
3. After 1 minute self-check, input Username (default: Adm) and Password (default: 123456) to login.
Test Procedure
➢ Software Operation
① ② ③ ④ ⑤ ⑥
A: Functions
B: Patient Info. E: Errors Info.
C: Result Display
F: Carousel Info.
D: Instrument Info.
Test Procedure
➢ Software Operation
4. Click“Reagent”button.
5. Insert the ID chip into the instrument.
6. Click“Read ID”button to memorize the information in the ID chip.
Test Procedure
➢ Software Operation
7. Click“Test”, a“Test”window will pop out. Edit the basic information and choose the sample
type and sample size.
8. Click“Add”button to add the Test request to“Wait Measuring List Area”.
9. Click“Edit”to enter the patient details.
Test Procedure
➢ Software Operation
10. Click“Start”to start the test, the access will automatically open.
11. The information“Please insert test device”will shown in“Instrument Info. Area”
Test Procedure
➢ Sample Adding
12. Open the package and take out the test device, draw the accurate sample volume which is in
accordance with the instructions of test kits to the buffer to mix thoroughly.
13. Add indicated volume of sample-buffer mixture into the sample well of Test Device, immediately
insert the test device into the holder.
Test Procedure
➢ Testing
14. Once the test device is inserted, the test device access closes. The carousel rotates to transfer
the test device into the test area. The bar code on the test device is then scanned. A time
countdown will appear on the screen.
15. When the test is finished, the results will show on the screen.
16. The test results will be automatic kept in the system,and can be query in “Test record” page.
Test Procedure
➢ Testing
17. Click “Print”to print the result. Also can export the result to the LIS system.
Test Procedure
➢ Stop Testing
17. After test, the instrument will automatically discard the test card, but if you want to manually kick
out the reagent card, here are two ways.
1) When the reagent card is shown in Carousel Info. area and start to countdown, click the regular
circle, then click“Discard card”button, the instrument will kick out that reagent card;
2) If want to kick out all the reagent card in the instrument, click“Test”, then click“Stop”button,
the instrument will immediately stop testing and kick out all the reagent cards in the instrument;
Test Procedure
Test Procedure
➢ Notices — Sample
Incorrect sample type
Hemolysis sample, Contaminated sample, Blood sample 4℃ preserve
more than 3 days
Incorrect sample storage and/or transport
Insufficient or excessive sample
Test Procedure
➢ Notices — Operation
Be aware of incubating at suitable temperature and in proper time
according to the instructions of test device
Lot number should match (cartridge, buffer, ID chip)
Rewarming to room temperature for 30 minutes. Open the package
after rewarming.
Accurate sample and mixture volume
Mixing thoroughly
Test Procedure
➢ Notices — Instrument
Please notice the insert direction of the reagent card. Incorrect
insertion can lead to serious consequences
The reagent card should be insert into position, after insert, hand
should be taken out immediately from the instrument.
When the access is running, please don’t touch the access or insert
the reagent.
Please insert the reagent card horizontally into the instrument
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