hemochroma PLUS is a handheld device that can run tests for anemia. One uses a disposable test cuvette to pick up sample blood from the fingertip. It accommodates tube bloods with a pipette. Each test takes 3~5 seconds and the user can transmit the result to a host computer.

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.

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.

MICROLET®NEXT Lancing Device NEW SIMPLY IMPROVED The easy-to-use MICROLET®NEXT lancing device is designed to help minimize pain so you can test with confidence. New and Improved Features to Love: Locking endcap helps prevent accidental lancing 5 clearly visible depth settings Smooth-gliding mechanism to minimize noise Easy-to-use lancet ejector Uses silicone-coated MICROLET®lancets for smooth gliding into the skin Uses MICROLET®Lancets Silicone coated for easier, gentler testing Available in Seven (7) vibrant colours to allow colour coded testing Coloured lancets give you visual feedback to remind you to change your lancets more often

INTENDED USE The Finecare™ Vitamin D Rapid Quantitative Test along with Finecare™ FIA Meter is a fluorescence immunoassay quantitative determination of total 25(OH) D2/D3 level in human serum or plasma. Results are to be used in conjunction with other clinical and laboratory data to assist the clinician in the assessment of vitamin D sufficiency. STORAGE AND STABILITY 1. Store at 4°C～30°C up to the expiration date. 2. The solid marker bottle can be stored at 2°C～8°C for 28 days after being reconstituted. 3. Do not remove the device from the pouch until ready to use. The Test Cartridges should be used within 1 hour once opened.

INTENDED USE The Finecare™ PSA Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative detemination of Prostate Specific Antigen (PSA) in human whole blood, serum or plasma. The test is used as an aid in diagnosis of prostatic cancer. STORAGE AND STABILITY 1. Store the test kit at 4~30℃ up to the expiration date 2. If removed from refrigerator, allow the test for 30 minutes to return to room temperature before testing. 3. Do not remove the device from the pouch until ready to use. The test cartridge should be used within 1 hour once opened.

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#Immunoassay #Reagents #Biotechnology #LifeScience #Biochemistry #Research #LabLife #Science #AssayDevelopment #Antibodies #Proteins #DiagnosticTesting #ClinicalChemistry #Laboratory #MedicalResearch #Healthcare #ELISA #Fluorescence #Chemiluminescence #Immunology #MolecularBiology #CellBiology #AnalyticalChemistry #Microbiology #BiomedicalScience #Diagnostics #Innovation #Technology #PrecisionMedicine #Biopharmaceuticals #BiomedicalResearch #Bioreagents #Pathology #Immunodiagnosis #Antigen #AntibodyDetection #ResearchAndDevelopment #ClinicalTrials #HealthTech #Biomarkers #MedicalDevices #PrecisionHealth #BiomedicalEngineering #Therapeutics #Pharmaceuticals #DrugDiscovery #Genomics #Virology #Microarray #PCR #FlowCytometry #Biosensors #Nanotechnology #Immunochemistry #MedicalDevices #MedicalTechnology #HealthInnovation #BiotechStartup #HealthTechInnovation #MedicalInnovation #HealthScience #BiomedicalDevices #HealthcareTechnology #LabResearch #Bioassay #Bioinformatics #ClinicalLaboratory #AssayKit #PointOfCare #LaboratoryMedicine #DiagnosticKits #Chemistry #BiomedicalDiagnosis #BiochemicalAnalysis #Immunodiagnostics #InfectiousDiseases #BiomedicalTechnology #DiagnosticInstruments #HealthcareInnovation #MolecularDiagnostics #MedicalInstruments #InVitroDiagnostics #BiomedicalInnovation #ClinicalChemistry #BiomedicalTesting #BiomedicalDevices #HealthcareTechnology #DiagnosticSolutions #BiomedicalSolutions #LabEquipment #HealthcareDevices #BiomedicalDevices #DiagnosticDevices #MedicalDevices #BiomedicalTools #LabTools #ResearchTools #LabSupplies #LaboratoryEquipment #ResearchEquipment

INTENDED USE The Finecare™ One Step cTn I/CK-MB/Myo Rapid Quantitative Test a fluorescence immunoassay to be used along with Finecare™ FIA System for quantitative determination of cardiac Troponin I (cTn I), MB Isoenzyme of Creatine Kinase (CK-MB) and Myoglobin (Myo) in human whole blood, serum or plasma. The test is used as an aid to the diagnosis of myocardial infarction. STORAGE AND STABILITY 1. Store Finecare™ One Step cTn I/CK-MB/Myo Rapid Quantitative Test at 4 ℃~30 ℃. Do not freeze. Shelf life is up to 24 months, refer to label for expiration date 2. If removed from refrigeration, allow the Test Cartridge for 30 minutes to reach room temperature (25±2℃) before testing. 3. Once opened, commence to use the Test Cartridge within an hour. 4. Do not remove the device from the pouch until ready to use. Keep the Test Cartridges away from light.