FIA8000 Quantitative Immunoassay Analyzer User Manual
Contents
1. Click on the Count icon to switch to Count Input Mode Set Count when ID is not 0 and Count will minus one automatically after each measurement and ID number will increase automatically until the Count value is zero F MEASURE 000000000 ount D000 D0000000 Fig 5 ID set interface In Fig 6 interface add sample to kit vertically and keep the sample at room temperature for a period of time then insert it into the analyzer when hear click sound it indicates the test kit have been placed in the correct location at this time click Measure icon or press ENT button the analyzer will automatically scan the kit and determine the item see Fig 6 When the test finished the analyzer will display measurement results and save the current measuring time number and other information as shown in Fig 7 Note refer to the sample volume and the test time of different items according to test kit FAs ss Measure Item Results Measure No 00002 Instruction Measure ID 000000000 Barcode Scanning Cancel Outside Measure S P ID Number Fig 6 Measurement interface 10 CE GP eelein pianooo ee Measure Item Results Measure No 00001 hs CRP O5 nsl Measure ID 000000001 Measure Time 2014 10 10 10 20 10 Barcode Outside Mode Cancel Outside Measure S P ID Numb2. p 0 CysC 10 8 MG 10 ii IN IN I Creatine Kinase MB CK MB 2 50 80 00 ng ml lt 1 8 BioMedical Inc CE OE ad GeTein 5 Warnings and srecautions a Only used for n Vitro diagnostic analysis of human whole blood plasma serum and Urine b Only the test kits mentioned in this instruction manual can be adopted otherwise the obtained results might be unreliable c Read this instruction manual carefully before operating and keep it properly for future use d If the analyzer gives off an unusual smell or smoke cut off the power and contact with service engineers immediately otherwise it would result in a fire electric shock or personal injury e If any liquid enters in the interior of the analyzer cut off the power and contact with service engineers immediately otherwise it would result in a fire electric shock or personal injury f Take proper safeguard measures according to health and safety standards in local country g Wear protective goggles surgery gloves and laboratory coat don t touch the patients blood samples directly and obey lab safety regulations to avoid the potential biological pollution risks of samples and reagents h The test kits and transfer pipettes should be discarded after single use as patients samples used test kits and transfer pipettes may be infectious Proper handling and disposal method should be established by the laboratory director in accorda
3. 3 Keypad UNCON inna E E a 3 3 4 Technical SP CifICATION cccscccccccesseececceeeeccecsueecccesausececseuaseeceesauaeceessauasecessuaaeeeeesauees 3 af NORV CS Ct AC LOIS CS eesosa a T a T A 5 AA Quality COMO OF FIRGCOOO sorreraren neia ona NERA AEAEE EAEE 5 4 2 Performance characteristics Of Matching test items ccesccccccsssseceecseeseccecseeseeceesaaaesees 5 5 Warnings ANd PrecCautiOns ccccccccsssseececceessccccceeeseccccceaeeceeseuaecceessuaseceessuaeceessuuaseceeseaaeeeesegees 6 i HIS CIN AU OM i E E E E E tae E I E E E E A 7 EAA D oe E A E A E nea A E E A 7 eZ F OWEN O er E E E E E E TE 7 6 3 Install printing paper esssssessseeeesssseerssssrerssssrerssssrerssssreresssreresssreressseeresssseresssreresssereresseeee 7 lt Operaune the FIA80OO x caivs cucscsswasiracivanwaresnecsuad a a a E 8 7 1 Preparations before power On ssiesssncscaasencaicanswassldnsavassiconsnnewdesanadseuusisacsdeasvataisanswaredbsabedelsenswnduns 8 PL POWOT O ia E AE A A EO E OAE A E A E 8 7 ded INE MININ Er aC sieer eaaa eaa a aeniea 8 Tie SAVING CONC HON rence a E a Ea 9 P SAV E OC a A E A O E A 9 7A Sample QUEE S nna EE E EA 11 7 3 SN tdoWA ACTION ncaseascserancwacedviatoavtanciteassatenetaanatenhoastsaetaauatsatenebanstnsnpeasionetaoeavenseawaaseseoehwoad 12 Oe MUN Sates O E A N AE N EE E aston os E E case aaueas N A E E N 12 EEE EE a a EE E EEE E E T 12 8 1 1 Auto Upload Auto Lis eeeeeeeerrrrrrrrrrrrrrrrrrrrrrrrrrrrrre
4. PCT 15 Min aan NT proBNP 15Min mAlb E 03 Min fag hs CRP s 1 5 Min NGAL e 03 Min ag cTnI NI proBNP 18 Min CysC iy 03 Min F CK MB cTn1 Myo 15 Min Buc Dobai D Dimer b ov Min h cTnI les 15 Min aa Cancel Next OK Fig 27 Display board interface 8 2 4 No Zero The No Zero function allows you to record No of tests and count from zero Click the No Zero as shown in Fig 28 interface and continue to click OK to achieve No zero as shown in Fig 29 F A8000 ac CIEE QC SD No Zero QC Card No 00000 rs Reac Time Cancel OK No Zero Manual Cal Cancel Fig 28 Zero No interface 22 CE GP elein F IA8000 ac CIEE QC SD No Zero QC Card No 00000 OK Reac Time No Zero Manual Cal Cancel Fig 29 Number zero success interface 8 3 Debug interface Debug interface is only used for factory debug 23 BioMedical Inc CE OE ad GeTein 9 Communication 9 1 Overview Upper Computer Software of FIA8000 Series Quantitative Immunoassay Analyzer hereinafter referred to as the PC software can communicate with and transfer data and the set parameters to FIA8000 Series Quantitative Immunoassay Analyzer it also can display real time circumstance of the Analyzer PC software also can be used to build modify and save user database search
5. enter the main interface as shown in Fig 3 FiAsooo Measure Item Results Measure No 00001 hs CRP lt 0 5 mg L Measure ID 000000001 Measure Time 2014 10 10 10 20 10 Cancel Outside Measure S P ID Number Fig 2 Boot screen 7 1 2 The main interface The main interface as shown in Fig 3 consists of five main modules Debug the debug interface QC Check quality control calibration Measure Search and Settings F LABOOU Quantitative Immunoassay Analyzer LEADING BRAND OF POCT Y a ms b Debug Settings ea QC Check 2011 03 23 20 07 52 Fig 3 The main interface 1 Debug It is used to adjust equipment parameters and common functions of testing 2 QC Check Set parameters of the analyzer ensure the accuracy of the measurement system 3 Measure Measurement of different items Operator can set the ID number types of CE AE AT exhibition board and sample 4 Search No and ID Results can be searched from the saved measurement results and be printed manually 5 Settings Set the commonly used functions of the analyzer 7 2 Sample collection WARNING DON T TOUCH THE PATIENT S BLOOD OR URINE sample Operators should treat patient s blood or urine samples carefully to avoid infectious diseases In order to avoid or reduce the related infection risks please use disposable gloves 7 3 Sample measurement Press the ENT button or touch
6. the Measure icon on the main interface and then enter the measure interface as shown in Fig 4 This interface includes sample mode exhibition mode ID Number the measurement icons Meanwhile Measure No Measure ID Barcode are also shown on the screen F Asoo0 ss Measure Item Results Measure No 00000 Measure ID 000000000 Measure Time Barcode Outside Mode Cancel Outside Measure S P ID Number Fig 4 Ready to measure interface 1 Sample mode clicking on S P icon to choose sample type including whole blood serum plasma and urine 2 Exhibition mode clicking on Outside or Inside icon switch exhibition mode including inside mode and outside mode Inside mode After sample is added to the detection tab the kit will be detected immediately after it is inserted into the analyzer click on the measure icon panel of the analyzer will countdown the measure time when time arrived the analyzer will detect the inserted kit automatically Outside mode After the sample is added to the detection tab keep it at room temperature for a period of time until the time arrives then insert the kit into the analyzer click on the Measure icon to determine the test kit J CE 7 GeTein E A BioMedical Inc 3 Measure Click on this icon start to measure corresponding item 4 ID Number Click this icon manually to set the desired ID Count as shown in Fig 5
7. 1 1 Identification analyzer FIA8000 Quantitative Immunoassay Analyzer Abbr used in the manual FIA8000 1 2 Product classification When classified by protection against electric shock FIA8000 is in transient over voltage Class Il When classified by pollution grade FIA8000 is in rated pollution degree 2 When classified by working system FIA8000 is a continuous running analyzer 1 3 Environment conditions Working environment Temperature 15 C 35 C Relative humidity 10 85 Air pressure 70 0kPa 106 0kPa Environment limitation in transport and storage process Temperature 15 C 40 C Relative humidity lt 93 Air pressure 50 0kPa 106 0kPa 1 4 Intended purpose The FIA8000 is an analyzer that used to measure biomarkers in human whole blood serum plasma or urine samples The test result can be used as an aid in clinical diagnosis The FIA8000 can be applied to laboratory and point of care testing Together with different test items the FIA8000 can be used to determine 10 different biomarkers in human blood quantitatively 1 cTnl 2 NT proBNP 3 hs CRP 4 CK MB 5 Myo 6 D Dimer 7 PCT 8 CysC 9 mAlb 10 B2 MG 1 5 Matching test kits The test items listed below are used to determine the concentration of corresponding biomarker by FIA8000 One Step Test for Cardiac Troponin Colloidal Gold One Step Test for NT proBNP Colloidal Gold One Step Test for hs CRP Colloidal Gold One Step Test for N
8. CE gF GeTein BioMedical Inc FIA8000 Quantitative Immunoassay Analyzer User Manual GeTein BioMedical Inc 4640 SW Macadam Avenue Suite 130C Portland OR 97239 USA Tel 1 971 407 3868 Fax 1 971 407 3868 E mail sales geteinbio com support geteinbio com Website http www geteinbio com Lotus Global Co Ltd 15 Alexandra Road London UK NW8 ODP Tel 44 20 75868010 Fax 44 20 79006187 CE GP celsi Catalogue Magoo lta o a A E E E A E E E E E E A E A E E E A gine cucu 1 TA JOS VICI CALION ccosheadenaes sa dacaateadeaneten ieonstoacsapeavadceas tosdcaeenuadesant TATTER 1 12 PROCUGE Class lMlGall OM seasiesnncacvantacecaicrucassomsaiadsen vudaevanduedyonnucnddnebatecrenuuanetmedasadvenunsncmednietueatink 1 L3 Environment COMGILIONS seisein enin na N EAE T EE 1 14 Intended pUrPOSE seiicennisnnrianiaii enni E A AEA AAA 1 1 5 Materials required but not provided ssesseeesssseensssseerrsssseressssrerssssrrrssserrresssreressereresses 1 Principle of measurem eNi escuramens ara a a a a E i 2 2 1 Overview Running a test cccecccssecceccesecceececsecceucessecceeeseeseeseeceseeseceeueesseceeaeesseseneensnses 2 2 2 Working principle ai ataba cinta cpeteetec stesso ceneeatpistssostda a a A AE 2 Package appearance and technical specification ccccccsssseecccceeseecceceeeseccecsueueeceesauaeceeseuaasees 3 SAPE EE a E EE E E E TE E 3 SE aE lll UN EIE A sien ccc are io ca E A A A A tenn eee esas 3
9. Fig 11 External barcode scanning interface 8 1 5 Auto Beep Auto Beep presents the current status of Auto beep v means the Auto beep is on otherwise it means off You can click Auto Beep to convert the status When the Auto Beep is on you will hear the sound of the keys when you click them 8 1 6 Date amp Time Date amp Time is mainly used to adjust the time In the interface showed as Fig 12 Click to add time click to reduce time Click OK to save these changes and back to the previous interface click Cancel icon to cancel the time setting and back to the previous pasooo o aly ar ih lt a L bnd J 2014Y 10M 04D 12H 41M 49S Cancel OK Fig 12 Date amp Time interface 8 1 7 Reset 14 C GFP GeTein EA BioMedical Inc If setup parameters have a difference or when you need to debug you can choose to restore the Reset It is not suggested to use Reset unless operated by professional and technical personnel Click the Reset icon as shown in Fig 13 interface then a dialog box pop out and shows Factory Reset Click OK to restore the factory settings then Factory Reset Success will pop out see Fig 14 Click on Cancel icon and exit this interface pasooo in Reset Auto Upload i Auto Scan n Cal Auto Screen Factory Reset Auto Print vi out Cancel OK Brightness i Sleep shi 15 Mi
10. T proBNP cTnl Colloidal Gold One Step Test for CK MB cTnl Myo Colloidal Gold One Step Test for D Dimer Colloidal Gold One Step Test for PCT Colloidal Gold One Step Test for CysC Colloidal Gold One Step Test for mAlb Colloidal Gold j One Step Test for B2 MG Colloidal Gold If you need them anytime please contact with your service engineers sa7o ago Dp CE GP celsi 2 Principle of measurement 2 1 Overview running a test After sample for example serum is added to the test kit insert the test kit into the FIA8000 and press ENT button Then the concentration of the selected item is be measured and displayed on the screen in a certain time The test result is stored in the FIA8000 and is available when required The result can also be transmitted to the lab or hospital information system through the LIS or HIS system when connected to FIA8000 2 2 Working principle The combination of the antigens in the sample the gold label antibody in the colloidal gold pad or nitrocellulose membrane and the antibody pre coated on the test line can form a purplish red streak on the test line The color intensity of the test line is proportionate to the quantity of antigens detected in the sample The analyzer system can obtain the photo electric signal intensity of the complex by scanning the test line with a photo electric component Then the voltage difference between the voltage of the test line and the background is obtaine
11. and browse data statistics and backup When use PC software during test some items with FIA8000 Series analyzer the user can real time observe experimental status and receive experimental data When the test finished user can input patients information and browse print the patient s test report 9 2 Software version Software name Upper Computer Software of FIA8000 Series Quantitative Immunoassay Analyzer Model FIA8000 Version V1 1 0 9 3 Environmental requirements Hardware environment CPU 2 Pentium II RAM 2 1000MB Hard disk 2 10GB Display resolution is no less than 1024x768 Printer resolution is no less than 600x600dpi Software environment Windows XP Win7 9 4 Analyzer maintenance and troubleshooting 9 4 1 Analyzer maintenance a Please operate the analyzer following the requirements of the instruction manual to ensure the reliable long term work b Calibrate the analyzer periodically by QC card to ensure the results accurate c Preheat the analyzer for 20 minutes before testing samples to ensure the results accurate and reliable 24 C gP GeTein EA BioMedical Inc d Analyzer should be placed in stable temperature dry place e Wipe the surface of analyzer gently with a clean dry cloth regularly f Do not try to disassemble the analyzer Operation done by laypeople may damage the analyzer 9 4 2 Troubleshooting lf there is an abnormal circumstance occur when operating the analyzer the analyzer w
12. ation 3 4 Technical specification CE Power voltage Power AC DC adapter Operating wavelengths Measurement range Voltage resolution Keypad display Screen size Printer Data storage Data output gP GeTein E 4 BioMedical Inc AC 100 240V 50 60 Hz DC 12V 5A supplied via AC DC adapter in package 60 VA Model SKUN90W 03 approved according to IEC EN 60950 540 5nm OmV 4000mV 1mV 4 buttons 5 6 inch touch screen 640 480 Thermal printer 10000 data can be stored The concentration results and voltage results are obtained one of them can be selected to display on the screen BioMedical Inc CE GP GeTein 4 Performance characteristics 4 1 Quality control of FIA8000 a The voltage of background QC test kit should be 2 3500mV b The linear correlation coefficients r should be 2 0 990 within OmV 4000mV c The relative standard deviation CV of repeated measure should be lt 1 d The voltage difference of QC test kits of the same concentration within one hour should be falls in the range of 2 2 4 2 Performance characteristics of matching test items Performance Characteristics Measurement Intra assa Inter assa range precision precision Cardiac Troponin cTnl 0 50 50 00 ng ml lt 10 lt N terminal B type Ao 15 natriuretic peptide NT proBNP 100 35000 pg ml lt 1 precursor 5 5 5 5 15 0 0 High sensitivit J y hs CRP 0 5 200 0 mg L lt 10 lt 15 C reactive protein
13. d The voltage difference has a linear relationship with the antigen concentration which can be used to calculate the antigen concentration The relationship has been established and varying from the measured parameter In conclusion the antigen concentration in whole blood plasma serum urine can be calculated quantitatively in one step according to the color intensity of the test line CE GP celsi 3 Package appearance and technical specification 3 1 Package The FIA8000 and related items are provided in a single box The test kits are packed separately including instruction for use If you find any part missing or if you have any questions contact our agents in your area or contact us directly Packing List No Description Unit Quantity 1 Mainframe set 1 2 Power Wire pc 1 3 Printing Paper pc 1 4 CD pc 1 5 Data Cable pc 1 6 User s Manual pc 1 7 Product Qualification Certificate pc 1 8 QC kit pc 1 9 Barcode Scanner pc Optional 3 2 Appearance Dimensions LxWxH 250mm x 250mm x 120mm Weight 3 97 pounds 1 80 kg Appearance shown as Fig 1 Micro Printer Interface i SD card slot Fig 1 Appearance of FIA8000 3 3 Keypad functions ENT Used for start of measurement and the choose of various operation interface RET Used for return to the previous interface from the current interface status PRT Used for test the print function condition and manual printing measurement results QC Shortcut key for QC SD Oper
14. e Insert SD o Fig 19 Plug in SD interface QC CHECK QC SD QC Card Cancel Fig 20 Proper insert SD interface Click on OK icon the screen will show Loading status as shown in Fig 21 This procedure must not power off as to avoid losing data and failure of quality control 18 C GP GeTein EA BioMedical Inc QC SD Success or QC SD Failed dialog box will pop up after SD card is read as shown in Fig 22 a and Fig 22 b After the success of quality control the parameter will automatically store in the analyzer system if quality control is failed please check whether the SD card is inserted properly or something is wrong with SD card and so on F IA8000 a omc QC SD Loading QC Card Reac Time Manual Cal QC CHECK QC SD Qc SD QC Card QC SD Success Reac Time No Zero Manual Cal Fig 22 a Quality control SD success interface 19 CE GP elein F A8000 QC CHECK QC SD QC SD Failed QC Card Reac Time No Zero Manual Cal Cancel Fig 22 b Quality control SD failed interface 8 2 2 QC card In order to ensure the accuracy of measurement and the comparability of measured data the optical part of the analyzer also need to calibrate on a regular basis Click on the QC card icon as shown in Fig 23 inte
15. e version interface 8 1 10 Brightness Brightness is mainly used for adjusting the brightness degree of screen click to increase brightness of screen click to reduce the brightness of the screen which can be set according to user s preference 8 1 11 Sleep The analyzer will automatically turn off the screen backlight if no operation was done for a period of time and switch into power saving mode Click on the to increase the auto screen time click on the to reduce the auto screen time and time range can be set between 1 60 minutes 8 2 QC CHECK QC Check include QC SD QC kit and Reaction Time No Zero Manual calibration and so on as shown in Fig 18 F IA8000 ac ocx QC SD QC Card Reac Time No Zero Manual Cal Cancel Fig 18 Quality control interface 17 CE Ga woe 8 2 1 QC SD In order to ensure the accuracy of measurement and the comparability of measured data use the corresponding SD cards of different batches to calibrate the analyzer before test different batches of kits Do as the following introduction Click on QC Check icon on the main interface and enter QC CHECK interface then touch QC SD icon as shown in Fig 19 then Please Insert SD dialog will pop out When SD card is properly inserted into the slot press the OK icon to do the quality control as shown in Fig 20 F A8000 cc ock QC SD QC Card Pleas
16. er Fig 7 Measurement results interface 7 4 Sample queries In the main interface click the Search icon and enter the search interface see Fig 8 Searching has two ways No and ID number Number query is system default But you can click on Inquire ID and switch to the Inquire ID interface Fiasooo o Inquire No Inquire ID Enter No Test Results 1 2 3 0 Es _ 4 la 6 7 8 9 vpe ores SO Cancel Upload Print Clear Fig 8 Search display interface Operation 1 Touch Search icon to enter search interface see Fig 8 2 Click on the number 0 9 icons enter the No or ID number you want to search 3 Click on the OK icon to begin search Search result shown as Fig 9 4 Click on the Print icon to print the current search result Note 1 The analyzer has a capacity of 10000 samples results therefore you cannot enter more than 10000 items when queried 11 CE 2 3 4 you want to search F 1A8000 Test Results Inquire ID Enter No No 00002 Time 2014 11 06 hs CRP 20 9 ID 000000000 4 IS 2222 2 ng L Upload Print If no search results shown No Results dialog box will show 2 3 0 5 6 OK 8 9 GeTein BioMedical Inc GP Click on the or icon to see previous or next search results Click on the Clear icon you can clear the search information re ino
17. ill perform the alarm process and enter the alarm interface The name explanation and treatment measures of alarms are showed in the following Err01 Display board is invalid and C Line on the strip is too shallow or no C Line the solution Change a new card Err02 Inconsistent measurement items and samples the solution switch sample mode re measure Err03 The barcode on the card surface failed to be identified the solution Change a new card with a clear barcode Err05 Internal parameters error the solution Re QC SD or Reset If you have any questions regarding the use of this analyzer please contact with local agents or contact with Getein s service engineer directly 25 CE GP gelei 10 Labeling Symbols Labeling Symbols In vitro Blagnoste medical device Authorised representative in Consult instructions for use Caution consult Biological risks accompanying documents Symbol for Environment protection Waste electrical products should not be disposed of with household waste Please recycle where facilities exist Check with your local Authority or retailer for recycling advice This way up Keep away from rain I Maximum number of identical Fragile 4 packages which may be stacked on one another is 4 GeTein BioMedical Inc 4640 SW Macadam Avenue Suite 130C Portland OR 97239 USA Tel 1 971 407 3868 Fax 1 971 407 3868 E mail sales geteinbio com support geteinbio co
18. m Website http www geteinbio com Manufacturer Keep away from sunlight E ec rer Lotus Global Co Ltd Add 15 Alexandra Road London UK NW8 ODP Tel 44 20 75868010 Fax 44 20 79006187 Version WYQ8600 SM XX 02 26
19. n eed Cancel Fig 13 Factory Reset interface piason O S Reset Auto Upload ry Auto Scan n Cal Auto Screen Factory Reset Success Auto Print iv out Brightness te Sleep te 15 Min _ Cancel Fig 14 Factory Reset Success interface 8 1 8 Screen Cal The subtitles position may shift when the analyzer is used for a long time at this time you can re calibrate the screen Click on the Screen Cal icon and enter the interface of Fig 15 click on the cross center on the screen according to the instructions Five points located in the four corners and the center of the screen when five points have been calibrated the system will automatically 15 CE GP GeTein BioMedical Inc determine the deviation If the deviation is too big the system will calibrate again until meet the requirements Fig 16 Touch the screen at any place to exit the calibration interface Please click the cross center to complete the screen calibration Fig 15 Screen calibration interface Tap the screen at any point to return Fig 16 Calibration complete interface 8 1 9 About Click on the About icon to check the program version as is shown in Fig 17 16 CE GP Gerein Fiasooo te FIA8000 Quantitative Immunoassay Analyzer LEADING BRAND OF POCT V1 1 1 Copyright 2012 Getein Biotechnology All Rights Reserved Fig 17 Softwar
20. nce with local status and federal regulations BioMedical Inc CE OF ad GeTein 6 Installation 6 1 Unpack a Take the FIA8000 from the packing box and put it on the table or other flat surface b Avoid dusts vibrations noises and power interferences Avoid direct sunshine hot sources and wind c Open the packing box and check the packing list If you find any part missing or broken contact our agents in your area or contact us directly 6 2 Power on Using the adapter packed together with the FIA8000 Supply voltage must be within AC100V AC240V Frequency 50 60Hz a Remove the AC DC adapter from the box b Connect power and FIA8000 through the AC DC adapter 6 3 Install printing paper a Open the printer door b Put the printing paper into the printer facing down to the hot sensor of the printer Leave the rest part of the paper outside of the door and close the printer door CE OF ad GeTein BioMedical Inc 7 Operating the FIA8000 7 1 Preparations before power on Before power the system on make sure the system is ready to use Check the system as the following steps Check if the power supply is ready and connected safely Check if the printer is ready including the paper and paper installation 7 1 1 Power on 1 Turn on the power switch of the analyzer 2 The system will check its hardware automatically The self check procedure shows in Fig 2 3 After self check is finished the system will
21. o Screen is on and no operation is taken within a defined time system will close the screen backlight and enter screen saver mode Click any area of the screen or any keys to recover 8 1 3 Auto Print Auto Print presents the current status of Auto print v means the Auto print is on otherwise it means off You can click Auto Print to convert the status System default of Auto Print is on Machine will print the testing data automatically when it is on otherwise it won t You can also print the data manually 8 1 4 Auto Scan Auto Scan presents the current status of Auto scan v means the Auto scan is on otherwise it means off You can click Auto Scan to convert the status When the status of Auto Scan is on click Measure icon on the measuring interface Scanning will appear which represents that it is waiting to be scanned as shown in Fig 11 At this time you can scan the barcode to start the test or click Measure icon again to skip this step After barcode scanned barcode value will display in the right box of Barcode barcode value will be uploaded to the PC software system and display in the test results 13 CE GP Gelein pias ean Measure Item Results Measure No 00002 Measure ID 000000000 Measure Time Barcode Scanning Outside Mode Cancel Outside Measure S P ID Number
22. rerrrrrrrrrerrrererrrrrererrrrrrrrrrerrrees 13 o LZ AO TE CIN a ETEO E R 13 pes AUTO PIE oerein nT T ETTE S 13 a a SCM EE A E E A A N A A N 13 SMEs T BOC P N E T P N A A E A A A T 14 8 1 6 Date amp T ING rasesanancasacartecssateasaontasaseqadaeeaatasass ER RN RE RIE E ER e aSa 14 oA T E E OG E E E E E E E E A E N E E O E tds ead E E A cas 14 S Lo SC FOI IU OWA pna a EEE E A 15 s RT ADOUAT EA EA 16 S L LOBOSNCSS aiana T 17 CE GP celsi A B E ES E 00 E AE ace area ia caste ca nc A E A A E A NE E E E E T 17 CC PAE AE A E E EA A S E EE T 17 S2 OC D E AO EA 18 B22 OC CAR D a E E E O E 20 8 23 Reaction TIME svscsscvawssanadscacsnnvavensiendawiedsinawawesaicadniadsien oaviensiendauiedslonwawesatadsadsenwavenseadauiedsinnds 21 BL ANOS LO EN A EEEN EA AE AEEA AANE AEON 22 8 3 DODO STG AC E cennera eaii A EEANN 23 POTE S E E EE 24 9 1 OVOFVIEW seriinin cresian Nn EEEN EEE EEEE EE ATN TEE EANTA 24 FD SOW Al VE Oar E AA EEA 24 9 3 Environmental requirements sirasisnscrasaduscsatadulssvondasureiedeideunedaisanateidsanudaiarataseuss nedwssveladounbes 24 9 4 Analyzer maintenance and troubleshooting cccccsssssececceesseccecseesseceesseeeeceeseuaeeeeeseeees 24 9 4 1 Analyzer Maintenance ccccccsssseccccccssececcseseecccsscssececcseuseccccseuaseecessaaseescsseuaeess 24 AP WOU NOONE penaa E EE E AE A E EAE 25 10 Labeling SV ONS aries arcsec arrvapaaasscsnapiard iann E 26 BioMedical Inc CE OE ad GeTein 1 Introduction
23. rface the dialog box of Please Insert QC card will pop up After you insert QC card click on OK icon internal parameter of the system will calibrate the analyzer see Fig 24 If the light intensity falls in the normal range the calibration is successful see Fig 25 otherwise indicates failure as shown in Fig 26 F A8000 QC CHECK QC SD QC Card QC Card Please Insert QC Card o Reac Time Cancel OK No Zero Manual Cal Cancel Fig 23 Please Insert QC card interface 20 CE GP celei F IA8000 QC CHECK ooo TF Loading Reac Time No Zero Manual Cal Cancel Fig 24 Quality control card reading interface F A8000 P QC SD QC Success QC Card Reac Time No Zero Manual Cal Cancel Fig 25 QC success interface PIA 8000 QC CHECK QC Card QC Failed Reac Time No Zero Manual Cal Cancel Fig 26 QC failed interface 8 2 3 Reaction Time Desired reaction time can be manually adjusted in the interface of Reaction Time through time display panel Reaction time settings as shown in Fig 27 the system 21 C GeTein EA BioMedical Inc default time of all test items shows the normal reaction time and icon on the left and right side of test item respectively click to increase the reaction time click to reduce the reaction time F14 COO Reaction Time cThl o A 15 Min
24. ut the number 00002 CTA Fig 9 Number search interface 7 5 Shutdown action The power switch can be used to shut off the machine directly at any interface 8 Settings Operation system will be set up by manufacturer Considering customers convenience many parameters can be reset to meet different requirements of different laboratories 8 1 System settings Click on the Settings icon in the main interface and enter Settings interface see Fig 10 Settings interface includes Auto Upload Auto Lis Auto Screen Auto Print Auto Scan Auto Beep Date amp Time Reset Screen Cal About Brightness and Sleep Fig 10 System settings interface 12 piason CE er N 8 1 1 Auto Upload Auto Lis Auto Upload Auto Lis presents the current status of Auto upload Auto Lis v means the status of Auto upload Auto Lis is on otherwise it means off You can click Auto Upload Auto Lis to convert the status The default status of Auto Upload Auto Lis is off Auto Upload Auto Lis function can process measurement data collected by inferior machine and upload these data to PC software system PC software will store search and print these data 8 1 2 Auto Screen Auto Screen presents the current status of Auto screen v means the Auto screen is on otherwise it means off You can click Auto Screen to convert the status When the status of Aut
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