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

 THANK YOU!
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