INTENDED USE The Finecare™ S100β Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative determination of S100β in human serum, plasma or whole blood. The test is used as an aid to the assessment of the level of cerebral injury. STORAGE AND STABILITY 1. Store the test kit at 4 ~ 30 ℃ up to the expiration date printed on package. 2. If removed from refrigerator, allow the test kit for 30 minutes to return to room temperature before testing 3. Do not remove the Test Cartridge from the pouch until use. The Test Cartridge should be used within 1 hour once opened.

Getein 1100 is used to measure the concentration of biomarkers in human whole blood, serum, plasma, urine, nasal swab, or saliva samples. The results can be used as an aid in clinical diagnostics of laboratory and point-of-care testing. It is applicable in Emergency, critical care (ICU, CCU), outpatient, cardiology, inpatient wards, clinical laboratories, etc.

At Mindray, we pride ourselves on our dedication and experience in developing better solutions for small labs. Our new 3-part hematology analyzer is the culmination of that effort. It provides small labs with more confidence in results and less turnaround time. Features CBC+3-DIFF, 20 parameters +3 Histograms Throughput: up to 30 samples per hour 8.4 inch TFT touch screen Only three reagents needed Open vial sampling Large storage capacity: up to 50,000 samples Original QC, calibrators and reagents Automation Fully Automatic Instrument Name Hematology Analyzer Brand Mindray Differential Type 2-Part Usage/Application Clinical Number Of Chambers 1 Model Name/Number BC-10 Power Source Electric Voltage 240 V Frequency 50 Hz

Product Specification Model VSI-102 Usage Laboratory Display Digital pH Range 0-14 pH Type of PH Meter Table-Top Product Description We are the Leading Supplier of Temp MV Meter. pH: Range: O TO 14 pH Resolution: 0.01 pH Accuracy: 0.01 oG?(Relative) Temp.Comp: Automatic with temp. Probe & manual by keys Buffer Recognition: 4.oo,7.oo,9.20ph(automatic) slope adjustment: 80% to 120% byu derfault 100% Calibration: Manually mV(ORP): Range: 0 To ±1999mV Resolution: 1mV Accuracy: ±1 mV Caliobration: Manual Temperature: Range: 20C to 200C Resolution: o.1C Accuracy: ±0.2% Input Type: Pt 100 Calibratian: Manual Display: 16x2 alphanumeric lcd. Display Format:temp & ph or temp &orp simultaneously auto display of selected buffer Setting: By soft touch keys Storage: 1000 samples with date & time Interfacer: RS-232 centroes & computer Real Time Display: 24 hour mode with date Error Indication PH error, buffer error, orp error Power Supply 230 V±10% AC 50 HZ Digital Output: Serial RS-232 and Parallel Centronics Print Format: All Data and Date wise

We bring forth for our clients an excellent quality of Filter Paper Whatman with the best quality. These papers are processed by making use of optimum quality basic pulp material and advanced technology under the strict industry laid norms. Our offered papers are available in different specifications to meet the requirements of the clients. Product Details: Brand Whatman Type Qualitative Packaging Type Box Shape Round Diameter 110 mm Pattern Plain

Palm-sized, fitting easily into a doctor's bag or uniform pocket. The printer can be separated from the "PocketChem" analyzer, leaving it with a weight of just 180g. Corrective features for obtaining accurate test results Accurate readings can be obtained by eliminating the effects of chromaturia using the color correction test pad, by compensating measurements for the temperature of the surrounding environment using a built-in temperature sensor and by correcting specific gravity based on pH readings. Palm-sized analyzer driven by two batteries The analyzer is detachable from the printer. The analyzer is really portable and mobile. Simple operation. Just press the start button Measurement is performed by simply pressing the start button and placing a test strip. Test results can be simultaneously viewed on the display and printed out from the printer. Reliable test results with Creatinine correction Even with the use of spot urine, test results are reliable and are not affected by urine dilutions or concentrations. The P/C ration or A/C ratio is effective for the screening of renal diseases. Sample Urine Test strips AUTION Sticks/ Uriflet S (9UB)* / AUTION SCREEN * Except devices with 10V specifications Measurement items GLU (glucose), PRO (protein), BIL (bilirubin), URO (urobilinogen), S.G. (specific gravity), BLD (blood), PH (pH), KET (ketones), NIT (nitrite), LEU (leukocytes), CRE (creatinine) and ALB (albumin). Measurement principle Test strip: Dual wavelength reflectance method. (one wavelength for BLD measurement) Measurement wavelengths 3 wavelengths LED (565, 635, 760 nm) Sample supply method Manual dipping Measurement capacity 50 tests per hour Test strip reaction time About 60 seconds per test Measurement types Normal measurement and check measurement Display Custom LCD that displays information including type of test strip, measurement number (up to 4 digits), patient ID (up to 13 digits) and test results. Operator panel Panel sheet that provides 14 buttons including numeric buttons and start button. Memory capacity Test results for 100 samples External output Compliant with RS-232 C Measurement environment Temperature: 10 to 30 °C; Humidity: 30 to 60 % R.H. (non-condensing) *Temperature correction function used Dimensions 124 (W) x 81 (D) x 36 (H) mm Weight 180 g (without batteries) Power supply Instrument only: Two AA alkaline batteries or AC adapter Instrument with printer: AC adapter 7.5 V 3 A Power consumption 3 W Printer specifications Printer Thermal recording printer Printer paper High color development thermal paper (W 58 mm x φ26 mm) Dimensions 125 (W) x 133 (D) x 36 (H) mm Weight 180 g (without printer paper) Power supply AC adapter 7.5 V 3 A Power consumption 20 W

Buy AccuTest COVID-19 IgG/IgM Rapid Test (Pack of 10 Tests) Online. COVID-19 IgG/IgM Rapid Test Kit is a qualitative immuno chromatographic assay for the detection of IgG & IgM antibodies produced against COVID-19 virus in human whole blood/Serum/ Plasma. COVID-19 IgG/IgM Rapid Test Kit is only intended for initial screening and reactive samples should be confirmed by a supplemental assay. Intended Use: COVID-19 IgG/IgM Rapid Test Kit is a qualitative immuno chromatographic assay for the detection of IgG & IgM antibodies produced against COVID-19 virus in human whole blood/Serum/ Plasma. COVID-19 IgG/IgM Rapid Test Kit is only intended for initial screening and reactive samples should be confirmed by a supplemental assay. SUMMARY & TEST DESCRIPTION: COVID-19 [Coronavirus Disease- 2019] is an infectious disease caused by SARS-CoV2 [Severe Acute Respiratory Syndrome coronavirus 2] virus, which is a contagious, novel strain of CoronaVirus that emerged from Wuhan, China in December 2019, which grew as a pandemic threatening human survival across the globe. The virus is thought to be of zoonotic origin and likely to have spread from large seafood and animal markets by human-animal contact in the city of Wuhan, where consumption of such products is in large. The virus causes respiratory infection with symptoms including fatigue, fever, shortness of breath, respiratory failure, renal failure and death. Patients can become infected with SARS-CoV-2 virus by person-person contact (through contact with a contaminated environment or person). The young and old (and other immune-compromised individuals) are most at risk of serious complications; however, approximately 20% of those infected can develop a critical condition. COVID-19 IgG/IgM Rapid Test device utilizes Anti-human IgG and Anti-human IgM antibodies as the capture molecules. COVID-19 Recombinant Antigens-colloidal gold conjugate are used as detection antigen. Intended Use: COVID-19 IgG/IgM Rapid Test Kit is a qualitative immuno chromatographic assay for the detection of IgG & IgM antibodies produced against COVID-19 virus in human whole blood/Serum/ Plasma. COVID-19 IgG/IgM Rapid Test Kit is only intended for initial screening and reactive samples should be confirmed by a supplemental assay. SUMMARY & TEST DESCRIPTION: COVID-19 [Coronavirus Disease- 2019] is an infectious disease caused by SARS-CoV2 [Severe Acute Respiratory Syndrome coronavirus 2] virus, which is a contagious, novel strain of CoronaVirus that emerged from Wuhan, China in December 2019, which grew as a pandemic threatening human survival across the globe. The virus is thought to be of zoonotic origin and likely to have spread from large seafood and animal markets by human-animal contact in the city of Wuhan, where consumption of such products is in large. The virus causes respiratory infection with symptoms including fatigue, fever, shortness of breath, respiratory failure, renal failure and death. Patients can become infected with SARS-CoV-2 virus by person-person contact (through contact with a contaminated environment or person). The young and old (and other immune-compromised individuals) are most at risk of serious complications; however, approximately 20% of those infected can develop a critical condition. COVID-19 IgG/IgM Rapid Test device utilizes Anti-human IgG and Anti-human IgM antibodies as the capture molecules. COVID-19 Recombinant Antigens-colloidal gold conjugate are used as detection antigen. PRECAUTIONS & WARNING 1. This package insert must be read completely before performing thetest. Failuretofollow directions in insert may yield inaccurate test results. 2. Test results should be read between 10 and 15 minutes after aspecimenisapplied to the sample well. Results read after 20 minutes may giveerroneousresults.3. Do not open the sealed pouch until you are ready to conduct theassay.Onceopened, the cassettes should be used immediately. 4. Do not use expired devices. 5. Bring all reagents to room temperature (15-30°C) prior to use. 6. Do not mix components from different kits. Use only the buffer suppliedalongwith the kit. 7. Wear protective clothing and disposable gloves while handling thekit reagentsand clinical specimens. Wash hands thoroughly after performing thetest. 8. Do not smoke, drink, or eat in areas where specimens or kit reagents arebeinghandled. 9. Dispose of all specimens and materials used to performthe test as biohazardouswaste. 10. Handle the negative and positive controls in the same manner as patientspecimens for operator protection. 11. Do not perform the test in a room with strong air flow, i.e. an electricfanorstrong air-conditioning. 12. Do not touch result window. 13. Use only for in-vitro diagnostic purpose.

Buy AccuTest Vitamin D Rapid Card Test (10 Tests) Online from Accurex. The Vitamin D test kit consists of 25 AccuTest Vitamin D individually packed test, devices in foil pouches, 25 pipettes for collecting 10 ul of whole blood, 25 lancets, 1 Buffer Vial (Buffer 5 mL) with stabilizers and, thimerosal, 1 Package Insert. Vitamin D Fast test kit is a rapid chromatographic immunoassay for the semi quantitative detection of Vitamin D levels in human blood/serum. This Vitamin D test provides a preliminary screening test result. INTENDED USE AccuTest Vitamin D is a rapid chromatographic immunoassay for the semi quantitative detection of Vitamin D levels in human blood/serum. This assay provides only a preliminary screening test result. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. The performance characteristics of this assay have not been established in a pediatric population. PRINCIPLE AccuTest Vitamin D is based on the principle of a competitive enzyme immunoassay. The assay is based on the competition for 25-OH Vitamin D present in blood/serum sample and Vitamin D present on the test line for fixed number of antibody-gold conjugate. Depending upon the concentration of Vitamin D in blood/serum, there will be free antibody-gold conjugate molecules that will bind to Vitamin D on the test strip and will show a colored line in the test line zone. A control line is present in the test window to work as procedural control. PRECAUTIONS 1. For in vitro diagnostic use only. 2. The test is designed for use with human blood/serum only. 3. Reagents must be at room temperature (8⁰C – 30 ⁰C). 4. Do not use if test device packaging is open or damaged. 5. Do not use the product beyond expiration date. 6. Handle all specimens as potentially infectious. Proper handling and disposal methods should be used according to good laboratory practices. 7. Read test results for 10 minutes as required. Results may deteriorate and may not be consistent after 10 minutes. 8. In order to avoid variable results, mix the blood sample thoroughly. 9. A serum sample subjected to repeated freeze thaw cycles may give variable results Direction for Use PROCEDURE 1. Remove the cassette from the sealed pouch and place it on a hard flat surface with the view window facing up (use the cassette as soon as possible). 2. Using a micropipette, add 10 µl of whole blood or 5ul of serum sample directly into the rectangular specimen well (marked with Red drop) of the cassette. 3. Add 3 full drops of Buffer into the square buffer well of the cassette (Do not move the cassette after addition of buffer). 4. Let the cassette sit for 10 minutes and read your results immediately. Results may deteriorate after the 10 minute mark. Other Info STORAGE AND STABILITY The test device should be stored at 8 ⁰C – 30 ⁰C and will be stable until the expiration date stated on the package. The product is humidity sensitive and should be used immediately after being open. INTERPRETATION OF RESULTS Match the color of the test line with the chart provided.

Buy Dengue NS1 Antigen test (Pack of 10 test) from Accurex. This NS1 Antigen Rapid test contains: A Test device in aluminum pouch with a desiccant, Disposable dropper & Pack Insert. Dengue NS1 antigen test utilizes the human serum / plasma followed by solid-phase immuno-chromatographic technology for the qualitative detection of dengue virus NS1 antigen. The membrane strip of the kit contains pre coated anti-dengue NS1 monoclonal antibody on the test band region (T), & goat anti-mouse IgG is pre-coated on the control band region (C). EXPLANATION OF THE TEST Dengue NS1 antigen test utilizes the human serum / plasma followed by solid-phase immuno-chromatographic technology for the qualitative detection of dengue virus NS1 antigen. The membrane strip of the kit contains pre-coated anti-dengue NS1 monoclonal antibody on the test band region (T), and goat anti-mouse IgG is pre-coated on the control band region (C). During testing, if the sample containing dengue NS1 Ag, the complex of the antibody-dengueNS1 Ag-gold conjugate moves laterally on the membrane by capillary action. In this case, the colored band will appear on the membrane in test line (T). Control line (C) should always appear if the test procedure is performed properly PRECAUTIONS 1. For in-vitro diagnostic use only. Do not re-use the test device. 2. The instruction must be followed exactly to get accurate results. 3. Anyone performing an assay with this product must be trained in its use and must be experienced in laboratory procedures. 4. Do not eat or smoke while handling specimens. 5. Wear protective gloves while handling specimens. Wash hands thoroughly afterwards. 6. Avoid splashing or aerosol formation. 7. Clean up spills thoroughly using an appropriate disinfectant. 8. Decontaminate and dispose of all specimens, reaction waste, in a biohazard container. 9. Do not mix and interchange different specimen. 10. The presence of humidity may decrease the stability of the tests. Thus, carry out the test immediately after removing the device from the foil pouch. 11. Do not use it beyond the expiration date. SPECIMEN COLLECTION AND STORAGE Direction for Use 1. Place all specimens, test device and solution. Allow them to room temperature prior to testing (15~30 min.) 2. Please perform the test immediately after removing the device from the foil pouch. 3. With a disposable dropper, load 2-3 drops (50 to 75µl) of specimen into the sample well (S) in the test device. 4. Interpret the test results between 15~20 minutes. Do not read the results after 20 minutes. Other Info STORAGE & EXPIRATION 1) Dengue NS1 Antigen test should be stored between 4~30 ºC 2) Expiration date of this kit is 24 months after its manufacture date. LIMITATIONS OF THE TEST Dengue NS1 antigen test is designed for primary screening test of dengue virus NS1 antigen. Although this can provide fast and easy way to get a result, the testing do not completely exclude the possibility of false positive or negative result caused by various factor. So, refer to the result of the kit, please make a final decision with clinical manifestation, other test results and doctor’s view collectively.