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Mission 10U Urine Analysis Strips (100 Tests)

The Mission 10U urine reagent strips are designed for the rapid, semi-quantitative detection of multiple analytes in urine. These are commonly used in clinical settings, laboratories, and for diagnostic screening to monitor metabolic or systemic conditions.

Parameters Tested (10 Analyte Panel)

The Mission 10U typically tests for the following parameters:

1. Leukocytes: Detects white blood cells (signs of infection).

2. Nitrite: Screens for certain types of urinary tract infections (UTI).

3. Urobilinogen: Indicates potential liver or hemolytic diseases.

4. Protein: Screens for kidney function and renal disorders.

5. pH: Measures the acidity or alkalinity of the urine.

6. Blood: Detects hemoglobin or intact red blood cells.

7. Specific Gravity: Evaluates the concentration of the urine (hydration status).

8. Ketone: Monitors metabolic status (important for diabetic ketoacidosis).

9. Bilirubin: Indicates liver or gallbladder issues.

10. Glucose: Primary screen for diabetes mellitus.

Product Specifications Key Features

• High Sensitivity: Reliable detection levels for early diagnosis.

• Color Stability: Clear, distinct color changes for easier visual comparison against the chart.

• Comprehensive Screening: Provides a broad overview of a patient's health in under 2 minutes.

• Long Shelf Life: Usually 24 months from the date of manufacture.

Usage Instructions

1. Specimen Collection: Use a fresh, well-mixed urine sample collected in a clean container.

2. Dipping: Immerse the strip briefly (no more than 1 second) into the urine, ensuring all reagent pads are wet.

3. Removing Excess: Run the edge of the strip against the rim of the container to remove excess urine.

4. Reading: Compare the reagent pads to the color chart on the canister label at the exact times specified (e.g., 30 seconds for Glucose, 60 seconds for Protein, 120 seconds for Leukocytes).

Diagnostic Test Kit Dr Morepen Pregnancy Card-25 test Dr. Morepen Pregnancy Test Card (HCG-25 Pack)

The Dr. Morepen Pregnancy Test Card is a rapid, one-step diagnostic kit designed for the qualitative detection of Human Chorionic Gonadotropin (hCG) in urine. This 25-test pack is ideal for clinical settings, laboratories, and bulk distribution, providing professional-grade accuracy with the convenience of a rapid result format.

Technical Specifications (Excel-Ready) Detailed Parameters

• Early Detection: Highly sensitive membrane technology detects hCG levels as low as 20 mIU/mL, allowing for detection as early as the first day of a missed period.

• One-Step Procedure: Simple "drop and read" format minimizes user error and requires no additional laboratory equipment.

• Moisture Protection: Each card is individually foil-wrapped and includes a silica gel desiccant to prevent moisture-induced reagent degradation.

• Clear Reading: Features a distinct "C" (Control) line and "T" (Test) line for unambiguous result interpretation.

Performance Characteristics

• Specificity: Formulated with monoclonal antibodies that show zero cross-reactivity with structurally related hormones such as hLH, hFSH, and hTSH at high physiological levels.

• Prozone Limit: Designed to maintain accuracy even at extremely high hCG concentrations (up to 500,000 mIU/mL), preventing false negatives in advanced pregnancy.

• Visual Intensity: High-contrast pink/purple lines provide a $4+$ intensity score for positive results, ensuring visibility even in low-light environments.

Safety & Handling Information

• Sample Collection: For maximum accuracy, the first-morning urine sample is recommended as it contains the highest concentration of hCG.

• Storage: Store in a cool, dry place. Do not freeze. Reagents must reach room temperature before use if stored in a refrigerator.

• Disposal: Treat all used cassettes as biohazardous waste. Dispose of according to local biomedical waste management protocols.

• Verification: A visible line at the "C" (Control) position is mandatory for a valid test. If no line appears, the test is invalid regardless of the "T" line.

Dr. Morepen Pregnancy Kit, HCG Test Card 25 Pack, Rapid Pregnancy Detection, UPT Test Kit, Home Pregnancy Test Bulk, Diagnostic Pregnancy Card, Morepen HCG Cassette, Early Pregnancy Detection Kit.Description: High-sensitivity rapid pregnancy detection kit from Dr. Morepen. This bulk pack contains 25 individually sealed HCG test cassettes and droppers. Features a 20 mIU/mL sensitivity threshold and 99% accuracy rate. Delivers clear, reliable results in under 5 minutes. Perfect for hospitals, clinics, and pharmacies. ISO certified and trusted for early detection. No prescription required for OTC distribution.

Era Chloroscope with OT (Ortho-Tolidine) Solution

The Era Chloroscope is a precision diagnostic instrument designed for the rapid estimation of residual chlorine in drinking water, swimming pools, and industrial effluents. Utilizing the Ortho-Tolidine (OT) method, this kit provides a colorimetric comparison to ensure water safety and effective chlorination levels. It is an essential tool for public health departments, water treatment plants, and laboratory quality control.

 

Technical Specifications (Excel-Ready) Detailed Parameters

• Dual Chamber Design: The chloroscope features a viewing window where a "control" sample and the "treated" sample are placed side-by-side for perfect color matching.

• Integrated Color Scale: A non-fading, permanent color standard is embedded into the device, ranging from pale yellow (low chlorine) to deep orange/yellow (high chlorine).

• OT Solution Potency: Formulated with a stabilized Ortho-Tolidine reagent that ensures rapid color development without sediment formation.

• Portability: Housed in a rugged, lightweight thermocol or plastic box, making it suitable for field testing and rural water monitoring.

Performance Characteristics

• Instant Results: Immediate color reaction upon addition of the OT solution allows for real-time adjustments to chlorination systems.

• High Contrast: The color standards are calibrated to provide high contrast, making it easy to distinguish between 0.2 ppm (safe drinking level) and 0.5 ppm.

• Stability: The OT solution is resistant to mild temperature fluctuations, maintaining its reactive properties even in tropical climates.

• Versatility: Capable of detecting "Free Residual Chlorine" when read within 10 seconds, and "Total Chlorine" when read after 5 minutes.

Safety & Handling Information

• Chemical Safety: OT Solution contains Ortho-Tolidine, which is a known irritant. Avoid skin and eye contact. Use gloves and protective eyewear during testing.

• Inhalation: Use the kit in well-ventilated areas. Do not breathe in reagent vapors.

• Storage: Keep the reagent bottle tightly capped in a cool, dark place. Prolonged exposure to direct sunlight can degrade the OT solution, turning it brown and rendering it ineffective.

• Disposal: Dispose of the tested water sample by flushing with plenty of running water. Do not ingest the tested sample.

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Bioline Dengue NS1 Ag & IgG/IgM Ab Combo Test

This is a rapid, solid-phase immunochromatographic assay for the simultaneous detection of Dengue NS1 antigen and differential IgG/IgM antibodies in human whole blood. It serves as a comprehensive diagnostic tool covering all stages of infection, from early onset (NS1) to the convalescent phase (IgG/IgM).

Technical Specifications  Detailed Parameters

• Dual Detection: Identifies the NS1 virus protein (early infection) and antibodies (current/past infection) in one device.

• Target: Detects all four Dengue serotypes (DEN-1, 2, 3, and 4).

• Visual Interpretation: Clear, color-coded bands for "C" (Control), "G" (IgG), "M" (IgM), and "NS1".

• Diagnostic Window: NS1 is detectable from Day 1 of fever; IgM becomes detectable by Day 3–5.

Performance Characteristics

• NS1 Ag Sensitivity: 92.4%

• NS1 Ag Specificity: 98.4%

• IgG/IgM Sensitivity: 94.2%

• IgG/IgM Specificity: 96.4%

• Precision: High reproducibility across different batches with minimal cross-reactivity to other flaviviruses like Zika or Malaria.

Safety & Handling Information

• Standard Precautions: Treat all blood samples as potentially infectious; use gloves and lab coats.

• Disposal: Dispose of used cassettes and lancets in biohazard sharps containers.

• Moisture Sensitivity: Do not open the foil pouch until the moment of testing; humidity degrades the nitrocellulose membrane.

• Buffer Safety: The assay buffer contains 0.1% Sodium Azide; avoid skin contact or ingestion.

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(Short Description)

Product: Bioline Dengue NS1 & IgG/IgM Combo Test Kit (10 Tests)

Description: High-accuracy rapid diagnostic kit for Dengue virus detection. Features a dual-track cassette for simultaneous NS1 antigen and IgG/IgM antibody screening. Suitable for whole blood, serum, or plasma samples. Results in 15 mins. Reliable performance for clinical labs and hospitals. ISO/CE certified.

Dhiti/Oscar Blood Grouping Monoclonal Antibody Combi Pack. These details are standard for high-quality IgM-based serological reagents.Technical Specifications Detailed Product Parameters

• Sensitivity: Designed to detect even "weak" subgroups (such as $A_x$ or $D^{u}$) that may not react strongly with lesser quality reagents.

• Stability: The reagents are chemically stabilized to maintain high avidity throughout their entire shelf life (typically 24 months from manufacture).

• Prozone Effect: Formulated to avoid the "Prozone effect" (false negatives due to antibody excess), ensuring clear results even with high-concentration samples.

• Potency: Maintains reactivity at a temperature of 37°C for up to 5 days during transit, though long-term storage must be cold.

Performance Characteristics

• Avidity: * Anti-A: < 5 seconds with $A_1$ cells.

  • Anti-B: < 5 seconds with B cells.

  • Anti-D: < 10 seconds with $O_{Rh}$ positive cells.

• Intensity: Provides a strong $4+$ agglutination score (large, distinct clumps with a clear background) for positive samples.

Safety & Handling Information

• Biohazards: Although the reagents are synthetic/monoclonal, they should be handled with standard biohazard precautions when mixed with human blood.

• Disposal: Due to the presence of Sodium Azide, disposal should involve flushing with large amounts of water to prevent lead or copper azide buildup in plumbing.

• Interference: Severe hemolysis or extremely high concentrations of serum proteins in the patient's blood may occasionally interfere with slide results; in such cases, a "washed cell" suspension is recommended.

Blood Grouping Kit Diagnostic Blood Group Test Kit Oscar Anti A,B,D (IgG-IgM) (3X 10ml) 

A Blood Grouping Kit is an essential diagnostic resource in clinical settings, emergency rooms, and blood banks. The accuracy of these kits is paramount, as a mismatch in blood types during medical procedures can lead to life-threatening hemolytic transfusion reactions.

Below is a detailed breakdown of the components, procedures, and scientific principles behind these kits.

Detailed Overview: Blood Grouping Kit Specifications The Science of Agglutination

The test relies on the biological principle of antigen-antibody interaction. Your red blood cells have "markers" called antigens. The kit provides "detectors" called antibodies.

How to Interpret Results

When the reagent (antibody) meets its matching antigen on the blood cell, they lock together, causing the cells to clump.

• Type A: Clumping occurs only in the Anti-A well.

• Type B: Clumping occurs only in the Anti-B well.

• Type AB: Clumping occurs in both Anti-A and Anti-B wells.

• Type O: No clumping occurs in either A or B wells.

• Rh Positive (+): Clumping occurs in the Anti-D well.

• Rh Negative (-): No clumping in the Anti-D well.

Importance in Healthcare and Safety

1. Transfusion Compatibility: Ensures that a recipient receives blood that their immune system will not attack.

2. Obstetric Care: Identifying the Rh factor in pregnant women is vital to prevent Erythroblastosis Fetalis (Rh incompatibility between mother and fetus).

3. Emergency Preparedness: Portable kits allow for rapid testing in field hospitals or disaster zones where lab access is limited.

4. Organ Transplantation: Matching blood types is the first step in determining donor-recipient compatibility.

Note: While home test kits are available for educational or personal interest, all clinical blood typing should be performed or verified by a certified laboratory professional to ensure patient safety.

Primary Keywords: Blood Grouping Kit, ABO Blood Typing, Rh Factor Test, Blood Agglutination Test, Blood Type Determination.

Secondary Keywords: Anti-A and Anti-B Reagents, Blood Group Test Procedure, Hemagglutination Assay, Blood Bank Diagnostic Tools, Rapid Blood Type Test.

Target Audience: Medical Professionals, Clinical Laboratories, Educational Institutions, and Emergency Response Teams.

Microgene AccuSure Pregnancy Card-20

The AccuSure Pregnancy Card by Microgene is a rapid, one-step diagnostic tool designed for the qualitative detection of Human Chorionic Gonadotropin (hCG) in urine. It provides a highly reliable and private way to confirm pregnancy within minutes of testing.Technical Specifications

Detailed Parameters & Performance

• Accuracy: Offers >99% clinical accuracy from the day of the expected period.

• Speed: Results are visible in 3 to 5 minutes.

   

• Limit of Detection: Highly sensitive to early pregnancy markers (25 mIU/ml).

• Clear Interpretation: Uses a two-line system (Control 'C' and Test 'T') for unambiguous reading.

Safety & Handling Information

• Single Use: Each card is for one-time use only; do not reuse.

• Moisture Sensitive: Open the foil pouch only when ready to perform the test.

• Hygiene: Dispose of the used card as per standard household or medical waste guidelines.

• External Use: For in-vitro diagnostic use only.

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Nanz HBsAg Cards (50 Test Pack)

The Nanz HBsAg Card is a rapid, one-step lateral flow immunochromatographic assay for the qualitative detection of Hepatitis B Surface Antigen (HBsAg) in human serum or plasma. It is a vital screening tool for identifying HBV infection in clinical and blood-bank settings. Technical Specifications

Detailed Parameters & Performance

• Principle: Utilizes the "Sandwich" immunoassay principle with monoclonal and polyclonal antibodies.

• High Sensitivity: Detects HBsAg at early stages of acute infection.

• Clear Interpretation: A distinct purple/pink "Test" line indicates a reactive result.

•  Internal Control: A built-in "Control" (C) line ensures the test functioned correctly.

   

Safety & Handling Information

• Biohazard Alert: Treat all blood derivatives as potentially infectious (HBV, HIV, HCV).

• Storage: Keep in sealed foil pouches until use; avoid high-humidity environments.

• Disposal: Autoclave or incinerate all used cards and samples according to biomedical waste rules.

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Nanz HIV 1/2 Card (50 Test Pack)

The Nanz HIV 1/2 Card is a rapid, qualitative, sandwich-based immunochromatographic assay. It is designed for the differential detection of antibodies to Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2) in human whole blood, serum, or plasma. It serves as a critical first-line screening tool for clinical diagnostics and blood safety.

Technical Specifications Detailed Parameters & Performance

• Antigen Source: Utilizes recombinant gp41/gp120 for HIV-1 and gp36 for HIV-2.

• Sensitivity: High clinical sensitivity (>99.9%) for early antibody detection.

• Specificity: High diagnostic specificity (>99.5%) with minimal cross-reactivity.

• Differential Detection: Features distinct test lines to differentiate between HIV-1 and HIV-2 infections.

• Control Mechanism: Includes an procedural control (C-line) to confirm valid test execution.

Safety & Handling Information

• Biohazard Protocol: Handle all specimens as potentially infectious; use gloves and protective gear.

• Single Use: Cards are strictly for one-time use to prevent cross-contamination.

• Storage: Keep in original sealed pouch until the moment of testing; avoid high humidity.

• Disposal: Dispose of used cards and lancets in puncture-proof biohazard containers according to local regulations.

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Nanz Malaria PF/PV Ag Test Kit (50 Tests)

The Nanz Malaria PF/PV Ag Card is a rapid, qualitative, and differential immunoassay for the detection of Plasmodium falciparum (Pf) and Plasmodium vivax (Pv) antigens in human whole blood. It utilizes HRP-II and pLDH markers to provide a high-speed diagnosis of malaria infections in clinical and field settings.

Technical Specifications Detailed Parameters & Performance

• Sensitivity: High sensitivity (approx. 98–99%), detecting as low as 50–100 parasites/µl.

• Differentiation: Distinct test lines for Pf and Pv allow for species-specific treatment.

• Accuracy: Correlates strongly with traditional microscopic blood smear analysis.

• Control Line: A built-in procedural control (C) ensures the reagent and device are functional.

Safety & Handling Information

• Biohazard Safety: Treat all blood samples and used test cards as infectious materials. Use gloves.

• Buffer Usage: Use only the assay diluent provided in the kit; do not substitute with other liquids.

• Environmental Limits: Do not use if the foil pouch is damaged. Avoid testing in areas with strong airflow (fans/AC) to prevent premature drying.

• Disposal: Dispose of lancets and used cards in biohazard-marked puncture-proof containers.

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 Nanz Syphilis Cards (50 Test Pack)

The Nanz Syphilis Card is a rapid, qualitative screening test for the detection of antibodies (IgG, IgM, and IgA) to Treponema pallidum (TP) in human serum or plasma. Using advanced immunochromatographic technology, it assists in the early diagnosis of Syphilis, a sexually transmitted infection.Technical Specifications

Detailed Parameters & Performance

• Antigen Utilization: Employs purified recombinant Syphilis antigens to ensure high reactivity.

• Sensitivity: Designed to detect TP antibodies at very low concentrations, ensuring early-stage screening.

• Specificity: Minimizes cross-reactivity with other non-related treponemal infections or biological interference.

• Visual Indicators: Features a two-line system (Control and Test) for easy, objective interpretation without lab equipment.

Safety & Handling Information

• Infection Control: All human-derived materials should be handled as if they are capable of transmitting disease.

• Integrity: Check the desiccant before use; do not use the kit if the foil pouch is punctured or damp.

• Professional Use: Intended for in-vitro diagnostic use by trained laboratory personnel.

• Waste Management: Treat all used materials as biohazardous waste and incinerate or autoclave according to regulatory standards.

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Nanz Typhoid (IgG/IgM) Card (50 Test Pack)

The Nanz Typhoid IgG/IgM Card is a rapid, qualitative immunochromatographic assay for the simultaneous detection and differentiation of IgG and IgM antibodies to Salmonella typhi and Salmonella paratyphi in human serum, plasma, or whole blood. It is an essential tool for the early diagnosis of Typhoid fever (Enteric fever).

Technical Specifications Detailed Parameters & Performance

• Differential Detection: Features three separate lines: Control (C), IgG, and IgM.

• Infection Stage: IgM detection indicates recent/acute infection; IgG detection suggests late or past infection.

• High Accuracy: Optimized with specific S. typhi antigens to minimize cross-reactivity with other enterobacteria.

• Reliability: Includes a built-in procedural control line to verify valid test performance.

Safety & Handling Information

• Infection Control: Treat all blood-based specimens as potentially infectious; use standard biosafety precautions.

• Buffer Management: Ensure the correct volume of assay buffer is added to the specimen well for accurate capillary flow.

• Storage: Keep the cards in the original sealed foil pouch until the moment of testing to prevent moisture damage.

• Disposal: Dispose of all used test components in biohazard-labeled puncture-proof containers.

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Sunsure HCV Cards (50 Test Pack)

The Sunsure HCV Card is a rapid, qualitative lateral flow immunochromatographic assay used to detect antibodies to the Hepatitis C Virus (HCV) in human whole blood, serum, or plasma. Utilizing highly purified recombinant proteins (Core, NS3, NS4, and NS5), it serves as a sensitive and reliable screening tool for the early identification of HCV infection.

Technical Specifications Detailed Parameters & Performance

• Advanced Reagents: Employs highly purified recombinant proteins: Core, NS3, NS4, and NS5 for superior binding.

• Clinical Sensitivity: 98.7% (detects low-level antibodies effectively).

• Clinical Specificity: 99.0% (reduces the risk of false-positive results).

• Reading Time: Clear results appear within 5 to 20 minutes.

• Reliability: Includes an internal procedural control (C line) to verify the test's validity.

Safety & Handling Information

• Specimen Safety: Treat all human blood components as potentially infectious (HBV/HIV/HCV). Use PPE.

• Storage Protocol: Do not freeze; store in a dry place. Keep in sealed foil pouches until the moment of testing.

• Ambient Conditions: Perform tests at room temperature; extreme heat or humidity may affect the lateral flow.

• Disposal: Autoclave or incinerate all used cards, lancets, and samples as per biomedical waste management guidelines.

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Biowick Glu+Pro Urine Test Strips (100 Tests)

Biowick Glu+Pro strips are high-precision diagnostic dipsticks designed for the rapid, semi-quantitative detection of Glucose and Protein in human urine. They serve as a primary screening tool for monitoring renal function, managing diabetes, and identifying early metabolic or kidney-related concerns.

Technical Specifications Detailed Parameters & Performance

• Glucose (GLU): Employs a double sequential enzyme reaction (Glucose Oxidase/Peroxidase). Detects levels as low as 50–100 mg/dL.

• Protein (PRO): Based on the "protein-error-of-indicators" principle. Highly sensitive to Albumin; detects as low as 15 mg/dL.

• Accuracy: >98% correlation with standard laboratory liquid chemistry.

• Interference: Optimized to minimize false results from common substances like Vitamin C (Ascorbic acid).

Safety & Handling Information

• Moisture Protection: Keep the bottle tightly capped. Reagent pads are highly sensitive to humidity.

• Avoid Contamination: Do not touch the reagent areas of the strip.

• Sample Integrity: Use fresh, well-mixed urine in a clean, dry container.

• Light Sensitivity: Keep away from direct sunlight to prevent reagent oxidation.

Primary Keywords: Biowick Urine Test Strips, Glucose Protein Urine Strip, Biowick Glu Pro 2P, Urinalysis Reagent Strips 100s.

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Keto-Diastix Reagent Strips

Keto-Diastix are high-quality diagnostic reagent strips designed for the simultaneous monitoring of Glucose and Ketone (Acetoacetic Acid) levels in urine. These strips are an essential tool for individuals with diabetes to manage glycemic control and detect early signs of ketosis or ketoacidosis.

Technical Specifications Detailed Parameters & Performance

• Glucose Performance: Utilizes the Glucose Oxidase/Peroxidase reaction. The color changes from light blue to dark brown based on concentration.

• Ketone Performance: Based on the Nitroprusside reaction. Specifically detects Acetoacetic acid, changing from buff-pink to deep purple.

• Sensitivity: Highly sensitive to metabolic shifts, allowing for proactive adjustment of insulin or diet.

• Consistency: Provides standardized color charts on every bottle for reliable semi-quantitative visual reading.

Safety & Handling Information

• Cap Integrity: Always replace the bottle cap immediately and tightly after removing a strip to prevent moisture contamination.

• Handling: Do not touch the reagent pads with fingers. Avoid getting urine on the hands by using a clean collection container.

• Expiration: Check the "Discard Date" (usually 6 months after opening). Do not use expired strips as reagents may oxidize.

• Storage: Keep away from direct sunlight, heat, and moisture. Do not store in the refrigerator.

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Diagnostic Urine Test Strips Peerless Mission 2GE Glu+Pro-100 test Peerless Mission 2GE (Glu+Pro) Urine Test StripsThe Peerless Mission 2GE is a specialized 2-parameter reagent strip designed for the rapid, semi-quantitative detection of Glucose and Protein in urine. These strips are a gold standard for point-of-care REAGENT STRIPS1. Mission – G (for Glucose)2. Mission – GP (for Glucose and Protein)3. Mission – GK (for Glucose and Ketone)4. Mission – 2CE (for Creatinine and MicroAlbumin)5. Mission – 3P (for Glucose, Protein & Ketone)6. Mission – 4P (for Glucose, Proteins, pH & SG)7. Mission – 10P (Glucose, Ketone, Blood, Protein, Leukocytes, Nitrite, pH, SG, Bilirubin & Urobilinogen)8. Mission – 14P (for Leukocytes, Urobilinogen, Albumin, Protein, Bilirubin, Glucose, Ascorbic Acid, SG, Ketone, Nitrite, Creatinine, pH, Blood & Calcium.) screening, particularly for monitoring diabetic patients and assessing early-stage renal (kidney) dysfunction in clinical settings.Technical Specifications Detailed Parameters & Performance

• Glucose (GLU): Uses Glucose Oxidase and Peroxidase. Detects glucose levels starting from 50 mg/dL, turning the pad from light green to dark brown.

• Protein (PRO): Highly sensitive to Albumin. Detects protein concentrations as low as 15 mg/dL (Trace), changing from yellow to dark green/blue.

• Accuracy: Engineered to provide high correlation with automated urinary analyzers.

• Reliability: Minimal interference from pH variations or specific gravity, ensuring consistent readings across different patient samples.

Safety & Handling Information

• Moisture Sensitivity: Reagent pads are extremely hygroscopic. Always replace the cap tightly and immediately after removing a strip.

• Handling: Do not touch the test areas of the strip with your hands. Hold the strip by the plastic end only.

• Specimen Quality: Use a fresh, mid-stream urine sample collected in a clean, detergent-free container.

• Disposal: Treat all used strips as biohazardous material and dispose of them according to your facility's medical waste guidelines.

Primary Keywords: Mission 2GE Urine Strips, Peerless Mission Glu Pro, Glucose Protein Urine Test, 2 Parameter Urinalysis Strip 100 Pack.

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Peerless Mission 10U Urine Test Strips (100 Tests)

Peerless Mission 10U is a comprehensive, 10-parameter diagnostic reagent strip designed for rapid urinalysis. These strips provide a "liquid biopsy" of the patient’s metabolic and renal status, offering a quick and reliable screening for UTIs, kidney disorders, and glucose metabolism issues in clinical or home settings.

Technical Specifications Detailed Parameters & Performance

• 10 Parameters Included: Leukocytes, Nitrite, Urobilinogen, Protein, pH, Blood, Specific Gravity, Ketone, Bilirubin, and Glucose.

• Accuracy: High correlation with automated analyzers and microscopic examination.

• Sensitivity: Detects early-stage changes in urinary chemistry, such as trace protein (15 mg/dL) or micro-hematuria.

• Consistency: Each reagent pad is treated to prevent "bleeding" or color run-over between adjacent test areas.

Safety & Handling Information

• Strict Closure: Re-cap the bottle immediately after removing a strip to prevent atmospheric moisture from deactivating reagents.

• Light Protection: Store in the original opaque bottle; do not expose strips to direct sunlight.

• Hygiene: Handle with gloves. Ensure the strip does not touch the urine container to avoid contamination.

• Reading Window: Do not read results after 2 minutes; color changes after this period are diagnosticially irrelevant.

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