Item Description The Accu-Chek Safe-T-Pro Uno lancing device keeps up with increased safety and hygienic requirements by health authorities, legislators, and health institutions. At the same time, it provides an ergonomic handling, lancing in just 3 milliseconds, and safety features that prevent accidental needle sticks. Its pre-set lancing depth makes it ready to use immediately. Benefits and Features Ready to use with a pre-set depth setting Safe-T-Technology ensures the needle is always safely stored away Stored needle prevents accidental needle sticks Ergonomical and easy to grip for safe handling Hygienic - each lancet can only be used once Beveled needle and small diameter for virtually pain-free blood sampling Equally suitable for right and left-handed use After a single use, the complete lancing device is disposed of Additional specifications Pre-fixed depth setting: Yes Penetration depth: 1.5 mm Needle diameter : 0.36 mm (28 G) Special needle cut: 3-facet cut Siliconized needle: Yes Sterility : 4 years after sterilization Single-use only: Yes Automatic retraction of needle : Yes Recognition of used device : Yes Intuitive handling : Yes How to use the Accu-Chek Safe-T-Pro Uno Simple, 2-step lancing Twist the sterility cap one quarter turn and remove it. Hold the lancing device between your index finger, middle finger, and thumb. Press the lancing device firmly against the chosen puncture site. Using your thumb, press the release button down completely. Move the lancing device away from the puncture site and discard it.

Item Description The Accu-Chek Softclix lancing device can help make lancing easy. Its rotatable cap offers 11 fixed depth settings for different skin types. Clixmotion technology minimizes any painful side-to-side motion of the lancet, which is why this lancing device is virtually pain-free to use. Benefits and features Virtually pain-free lancing Clixmotion technology controls the lancet’s movement Less side-to-side motion of the lancet means less skin damage Turn the rotatable cap for 11 penetration depth settings for different skin types The Accu-Chek Softclix lancets are precisely manufactured for precise entry Additional specifications Penetration Depth: 11 fixed-depth options, set with the rotatable cap Penetration Range: 0.8 to 2.3 mm Lancing Technology: Clixmotion Technology Weight: 21 g Alternative Site Testing: AST cap provided Needle Diameter: 0.4 mm Gauge: 28 Coating: Silicon How to use the Accu-Chek Softclix lancing device The Accu-Chek Softclix lancing device is small and easy to operate, with one-hand priming and lancing. Pull off the cap. Insert a new lancet into the lancet holder and push it in until it clicks. Press the cap on again until it clicks. Rotate the cap until the desired penetration depth is set. Press the priming button down until it clicks. Press the lancing device firmly against the side of the fingertip. Press the yellow release button. After measuring your blood glucose, pull off the cap and slide the ejector forwards to remove the lancet.

Accu-Chek® Instant Blood glucose monitor Your effortless choice Item Description Wishing there was an easy way to monitor your blood glucose levels? With the new Accu-Chek Instant meter, it's as easy and fast as checking your phone messages. There is no setup required – just insert a test strip, apply a small blood sample and read your blood glucose result on the large display. Additional specifications Model: Accu‑Chek Instant wireless blood glucose meter​ Meter storage conditions: Temperature: -25 – 70° C Memory capacity: The meter automatically stores at least 720 blood glucose results in memory, but only the last blood glucose result and your 7, 30, and 90 day averages can be viewed on the meter. To view stored blood glucose results, transfer them to a compatible software application. The meter automatically stores at least 30 control results in memory, but only the current control result can be viewed on the meter. To view stored control results, transfer them to a compatible software application. Sample claims: Capillary: Yes Venous: Yes Arterial: Yes Neonate: Yes Non-fingerstick sample Claim: Palm, forearm, upper arm Measuring principle: FAD glucose dehydrogenase (GDH) Measuring time: 4 Sec Measuring conditions: 4 °C to 45 °C (39 °F to 113 °F) Hematocrit range: 10 to 65 % Humidity range: 10 to 90 % Altitude independence: 0 to 3,094 m (10,150 ft) Automatic off: 90 seconds after performing a test, 15 seconds after test strip is removed, or 5 seconds from the last test result screen. Weight: Approx. 40 g (with batteries) Construction: Hand-held Protection class: III Meter type: The Accu-Chek Instant meter is suitable for continuous operation. Interfaces: Connectivity using BLE wireless Technology to mySugr App; USB interface with USB cable to transfer data to the Accu‑Chek Connect Online system. Benefits and Features Effortless Bluetooth synchronization with mySugr diabetes management app The intuitive target range indicator gives you visual reassurance. It can be individualized to suit your personal therapy goals Only what you need: Your test result and your averages (7/30/90 days) are visible on the meter Sleek, modern design with large, easy-to-read BG numbers and a bright, backlit display No set up required – just insert a strip, apply a small blood sample, and read your blood glucose result on the large display Easy-edge test strip: Apply a small drop of blood anywhere along the wide, yellow edge Proven accuracy guaranteed by the makers of the Accu-Chek brand, fulfilling the requirements of the ISO 15197:2013, EN ISO 15197:2015 All data can be uploaded to the mySugr by using Bluetooth Low Energy wireless technology and to Accu-Chek Connect Online portal by using USB Test strips come in a 10, 25, 50 vial so you can choose whatever fits your budget or therapy Enjoy virtually pain-free testing with the Accu-Chek Softclix lancing device

Accu-Chek Instant S blood glucose meter Item Description Get instant clarity of your blood glucose level with Accu-Chek Instant S meter, it's as easy and fast as checking your phone messages. There is no setup required – just insert a test strip, apply a small blood sample and read your blood glucose result on the large display. Benefits and Features The Intuitive target range indicator gives you visual reassurance. It can be individualized to suit your personal therapy goals* Only what you need - Your test result and your averages (7/30/90 days) are visible on the meter No set up required – Just insert a strip, apply a small blood sample, and read your blood glucose result on the large display Easy-edge test strip - Apply a small drop of blood anywhere along the wide, yellow edge Proven accuracy guaranteed by the makers of the Accu-Chek brand, fulfilling the requirements of the ISO 15197:2013^ Test strips come in a 10, 25, 50 vial, so you can choose whatever fits your budget or therapy All data can be uploaded to the Accu-Chek Connect Online portal (USB) Enjoy virtually pain-free testing with the Accu-Chek Softclix lancing device Additional specifications Meter storage conditions: Temperature: -25° C to +70° C (39° F to 113° F) Memory capacity: The meter automatically stores at least 720 blood glucose results in memory, but only the last blood glucose result and your 7, 30, and 90 day averages can be viewed on the meter. To view stored blood glucose results, transfer them to Accu-Chek Connect Online diabetes management . Automatic off: 90 seconds after performing a test, 15 seconds after test strip is removed, or 5 seconds from the last test result screen. Weight: Approx. 40 g (with batteries) Construction: Hand-held Meter type: The Accu-Chek Instant S meter is suitable for continuous operation. Interfaces: USB: micro-B connector Serial number: Unique serial number etched into meter back Sample claims: Capillary: Yes Venous: Yes Arterial: Yes Neonate: Yes Measuring principle: FAD glucose dehydrogenase (GDH) Hematocrit range: 10 to 65 % Humidity range: 10 to 90 % Altitude independence: 0 to 3,094 m (10,150 ft) Measuring time: Less than 4 seconds Measuring conditions: 4° C to 45° C(39° F to 113° F)

Accu-Chek® Active blood glucose meter Personalised Diabetes Coaching Accurate, no coding, easy Item Description The Accu-Chek Active blood glucose meter packs many powerful features into a smaller size. No coding reduces handling steps, see test result averages up to 90 days, get alerts if your test strips are expired or if you’ve underdosed, re-dose within 10 seconds, set pre-and post-meal reminders to test, and more. Benefits and Features accurate: Accurate1 blood glucose measurement easy: No coding for even easier blood glucose monitoring easy-to-read display (new typeface) intuitive handling with just 2 buttons safe: Underdose detection visual double check 10 seconds re-dose option clever: Pre- and postmeal markers postprandial reminder 7,14,30 or now 90 day test averages USB interface for data transfer Remark: Previous Accu-Chek Active meter generations will be upgraded to no coding via black activation chip . Know more>> 1The Accu-Chek Active bGM system meets the DIN EN ISO 15197:2013 requirements (data on file, 2014). Additional specifications Meter type : Accu-Chek Active meter (Model GB) Catalogue no. / Serial no. : See type plate on the back of the meter Test principle : Determination of glucose in fresh capillary blood by reflectance photometry. Blood glucose values can be tested in whole blood or plasma. The meter displays blood glucose values corresponding to those in plasma. Measuring interval : 10-600 mg/dL Blood volume : 1-2 μl Measuring time : Test strip in the meter: approx. 5 seconds Test strip outside the meter: approx. 08 seconds Power supply : 1 battery (type CR2032) Battery life : approx. 1000 tests or approx. 1 year Automatic power-off : after 30 or 90 seconds depending on operating status Memory : 500 test results with time and date, as well as 7, 14, 30 and 90 days averages Temperature : During testing: +8 to +42°C During storage without battery: -25 to +70°C During storage with battery: -20 to +50°C Atmospheric humidity : During testing: up to 85% relative humidity During testing: up to 93% relative humidity Altitude: Sea level to 4000 m Dimensions : 97.8 x 46.8 x 19.1 mm Weight : Without battery: approx. 46 g With battery: approx. 50 g Display : 96-segment liquid crystal display (LCD) Interface : USB (Micro B) Safety class : III Electromagnetic compatibility : The Accu-Chek Active meter meets the electromagnetic immunity requirements and the electromagnetic emissions requirements as per EN 61326-2-6 and EN ISO 15197 Annex A. The chosen basis for electrostatic discharge immunity testing was basic standard IEC 61000-4-2. Performance analysis : Calibration and traceability: The performance data for the Accu-Chek Active bGM system was calibrated using venous blood containing various glucose concentrations. Reference values are obtained using the hexokinase method, which is calibrated using the ID-GCMS method. Accuracy performance : The Accu-Chek Active bGM system meets the DIN EN ISO 15197:2013 requirements (data on file, 2014). How to use Accu-Chek Active blood glucose meter Testing your blood glucose is an essential part of managing diabetes. The Accu-Chek Active blood glucose meter can help to make it convenient by giving you fast, hassle-free, and accurate results in 4 simple steps. Insert the glucose test strip Prick your finger with the lancet to draw out a blood drop. Carefully touch the blood drop onto the green field of the test strip. Read the blood glucose result.

Buy AccuTest Malaria Pf(HRP II)/Pv Rapid Card Test (50 Tests) Online from Accurex. This Malaria test is a rapid qualitative, chromatographic immunoassay for the detection of malaria infection in human blood sample indicating differential diagnosis between Plasmodium falciparum and Plasmodium vivax species. This Malaria parasite test kit has test strips coated with Monoclonal Anti-p LDH antibodies (test line Pv) specific to the lactate dehydrogenase of P. vivax species and the other (test line Pf) with Monoclonal Anti-HRP-II which is specific to the Histidine Rich Protein-II of P. falciparum. AccuTest Malaria Pf(HRP II)/Pv is a rapid qualitative, chromatographic immunoassay for the detection of malaria infection in human blood sample indicating differential diagnosis between Plasmodium falciparum and Plasmodium vivax species. PRINCIPLE: AccuTest Malaria Pf (HRP II)/Pv test utilizes the principle of immuno-chromatography. It has the test strip coated with Monoclonal Anti-pLDH antibodies (test line Pv) specific to the lactate dehydrogenase of P.vivax species and the other (test line Pf) with Monoclonal Anti-HRP-II which is specific to the Histidine Rich Protein-II of P.falciparum. As the test sample flows through the membrane assembly of the device after addition of the buffer solution, the colored colloidal gold, anti-pLDH antibody and the anti-HRP-II antibody conjugate complexes with the lysed blood sample. The Malaria antigens get immobilized on the respective test lines on the nitrocellulose membrane which leads to the formation of red/purple colored band/s. The un-reacted conjugate and unbound complex if any moves further on the membrane and are subsequently immobilized at the control “C” region forming a red/purple band. This control band serves to validate the test performance and should always appear. This test is intended for professional use and must be used by trained personnel. Related products Safety Information PRECAUTIONS: 1. For in-vitro diagnostic use only. 2. The device is sensitive to humidity as well as to heat. So, it’s very important to take out the device from the sealed pouch just before use. 3. Do not use the kit after the expiration date. 4. Dispose all the samples and kits properly after test, in accordance with GLP. 5. Do not pipette reagent or blood by mouth. Direction for Use Procedure: 1. Disinfect with alcohol swab 2. Punture by lancet 3. Collect blood upto marking on sample dropper Other Info STORAGE AND EXPIRATION: 1. AccuTest Malaria Pf(HRP II)/Pv test kit should be stored between 4 – 30ºC. 2. Expiration date of this kit is 18 months after its manufacture date.

Buy AccuTest HCV Rapid Card Test (30 Tests) Online from Accurex. HCV means Hepatitis C Virus which is a is a small, enveloped, positive-sense, single-stranded RNA virus. Hepatitis C symptoms are fever, fatigue, decreased appetite, nausea, vomiting, abdominal pain, dark urine, pale feces, joint pain and jaundice. HCV test is a rapid Chromatographic Immunoassay work on principle of the double antigen sandwich technique, Qualitative detection of antibodies generated against proteins that are encoded by conserved sequence of core NS3, NS4, NS5 parts of HCV genome in human whole blood/serum or plasma. AccuTest HCV Test is a rapid Chromatographic Immunoassay for the Qualitative detection of antibodies generated against proteins that are encoded by conserved sequence of core NS3, NS4, NS5 parts of HCV genome in human whole blood/serum or plasma. Hepatitis C Virus (HCV) is a small, enveloped, positive-sense, single-stranded RNA virus. Antibody to HCV is found in over 80% of patients with well documented non-A, non-B hepatitis. Conventional methods fail to isolate the virus in cell culture or visualize it by electron microscope. Cloning the viral genome has made it possible to develop serologic assays that use recombinant antigen, multiple antigens using recombinant protein and/or synthetic peptides have been added in new serologic tests to avoid nonspecific cross-reactivity to increase the sensitivity of HCV antibody tests. Storage and Stability: AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch. Test Procedure: 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or quest Principle: AccuTest HCV Rapid Hepatitis C Virus Test (Serum/Plasma/Whole Blood) is a lateral flow chromatographic immunoassay based on the principle of the double antigen-sandwich technique. The membrane is coated with recombinant HCV antigen on the test line region of the device. During testing, the serum/plasma or W.Blood specimen reacts with HCV antigen coated particles. The mixture migrates upward on the membrane chromatographically by capillary action to react with recombinant HCV antigen or membrane and generate a colored line. Presence of this colored line indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region, indicating that the correct volume of specimen has been added and membrane wicking has occurred. Storage and Stability: AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch. Test Procedure: 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or questionable results are obtained, the HCV infection is suspected, the test should be repeated ona fresh serum specimen. Safety Information •Positive: If a distinct purple line is formed at the test one marked ‘T’ (Test Line) and the Control Zone marked ‘C’ (Control Line) the test result is positive, indicating the sample contains Hepatitis C antibody. The interpretation of test results (+ve for hepatitis) remains unchanged even if there is a difference in intensity of color in positive line and control line as is many a time found. •Negative: If a distinct purple line is formed only at the control zone marked ‘C’ (control line) the test result is negative • Invalid: A total absence of color in both © and (T) regions or no colored band appears on the control © region is an indication of procedure error and/or the test reagent has deteriorated. Repeat with a new test kit. Direction for Use Test Procedure 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or questionable results are obtained, the HCV infection is suspected, the test should be repeated ona fresh serum specimen. Other Info Storage and Stability AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch.

Buy AccuTest HBsAg Rapid Card Test (50 Tests) Online from Accurex. HBsAg means Hepatitis B surface antigen which is a protein on the surface of hepatitis B virus. It can be detected in high levels in serum during acute or chronic hepatitis B virus infection. HBsAg positive indicates that the person is infectious. The hbsag test kit is a one-step immunochromatographic assay based on the antigen capture, or Sandwich principle. HBsAg positive treatment may include Antiviral medications. AccuTest HBsAg Card Test Hepatitis BHepatitis B is a viral infection that attacks the liver and can cause both acute and chronic disease. An estimated 240 million people are chronically infected with hepatitis B (defined as hepatitis B surface antigen positive for at least 6 months). Laboratory diagnosis of hepatitis B infection focuses on the detection of the hepatitis B surface antigen HBsAg. Hepatitis B surface antigen (HBsAg) consists of lipid carbohydrate and protein elements; the protein moiety provides a marker for identification of chronic, infectious BBV infections. Hepatitis B is transmitted sexually or intravenously and has an incubation period of six months. If not diagnosed properly and in time, it can develop into acute or chronic infection, liver cirrhosis and fulminant hepatitis. This test is very useful for screening blood donors, to find out whether they are HBsAg positive before collection of blood. Principle: AccuTest HBsAg is a qualitative test based on immunochromatography sandwich principle. The test card includes a combination of monoclonal anti-body gold conjugate (colloidal gold) and polyclonal solid phase antibodies which selectively binds Hepatitis B surface antigen with high degree of sensitivity. The HBsAg test is a one-step immunochromatographic assay based on the antigen capture, or Sandwich principle. The method uses monoclonal antibodies conjugated to colloidal gold and polyclonal antibodies immobilized on a nitrocellulose strip in a thin line. The test sample is introduced into well and flows laterally through an absorbent pad where it mixes with the signal reagent. If sample contains HBsAg, the colloidal gold-antibody (mouse) conjugate binds to the antigen, forming an antigen-antibody-colloidal gold complex. The complexes then migrate through the nitrocellulose strip by capillary action, which are stopped by an immobilized antibody zone forming a purple band. The formation of the first purple band (T zone) is indicative of hepatitis positive. To serve as a procedural control, an additional line of antibody antimouse IgG has been immobilized on the card. If the test is performed correctly, this will result in the formation of purple and upon contact with the conjugate as a control line. Safety Information AccuTest HBsAg test kit is designed lor detection of Hepalitis B Surface Antigenin the specimen. As with all diagnostic tests, il is recommended to interpret all the results in line wilh clinical manifestations, other lest resulls & clinicians’s view colleclively. If the lest device is showing stagnancy in flow on chromalography, it is most likely due lo problem in the sample. In this case, relest with a fresh sample or diluted sample. Direction for Use Test Procedure: 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (25 ul), wait for few seconds till the Whole blood absorbed by sample pad (approx. 30 second), 4. Add 2-3 drops of buffer (60 ul) into the sample well. (If needed add one more drop of assay buffer). 5. Let reaction proceed until the appearance of positive line and control line or up to 20 minutes. 6. Read results after 20 minutes, strong positive reaction may visible within 5 minutes. 7. If negative or questionable results are obtained, the HBV infection is suspected, the test should be repeated ona fresh serum specimen. Storage: AccuTest HBsAg should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch.

Buy Dengue NS1 Antigen test (Pack of 5 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. Dengue NS1 Antigen kit is for professional use and only for the initial screening test & reactive samples should be confirmed by a supplemental assay such as nucleic acid test & other immunological assays. 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 Safety Information 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. 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 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.