Dermatoscope and Magnifiers
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Kids & Novelties
Ready-to-use collections of tools, reagents, and components designed for efficient and accurate medical testing. These kits streamline the process of sample collection, analysis, and detection for various conditions, including infections, chronic diseases, and metabolic disorders. Common examples include rapid test kits, blood collection sets, culture kits, and molecular diagnostic assays. Ideal for clinics, laboratories, and point-of-care settings, they ensure reliability, consistency, and timely results.
Anti-Streptol Olysin O Titer (ASOT)
Anti-Streptol Olysin O Titer (ASOT) is a quantitative or semi-quantitative serological test (latex agglutination, turbidimetry, nephelometry, or ELISA) for detecting antibodies against streptolysin O, an exotoxin produced by Group A Streptococcus. Elevated or rising titers indicate recent streptococcal infection and are essential for diagnosing post-streptococcal sequelae including acute rheumatic fever (Jones criteria) and post-streptococcal glomerulonephritis. The test requires serum samples; acute and convalescent (2-4 weeks apart) with fourfold rise confirms recent infection. Reference range typically <200-250 Todd units/mL (adults), varies by age and population. Primary clinical applications include diagnosis of Group A streptococcal infections, acute rheumatic fever evaluation, post-streptococcal glomerulonephritis diagnosis, differentiation of acute vs. past infection, evaluation of unexplained arthritis or carditis, pediatric inflammatory conditions (PANDAS), and monitoring disease activity in rheumatic fever. Critical safety precautions include proper timing of acute and convalescent samples, awareness of false negatives/positives, clinical correlation for diagnosis, and standard biohazard precautions. Essential test for rheumatology, nephrology, cardiology, and infectious disease practice.
Applicator Sticks
Applicator Sticks are single-use medical devices with absorbent tips (cotton, rayon, flocked polyester) on wood, plastic, or paper shafts for collecting clinical specimens (throat, nasal, wound, cervical, urethral, rectal) for microbiological culture, rapid testing, and molecular diagnostics. Sterile individually wrapped or non-sterile bulk formats. Flocked swabs provide >90% specimen release for PCR testing. Primary applications include specimen collection for infection diagnosis, wound care and antiseptic application, gynecological sampling (Pap smears, STI testing), eye/ear specimen collection, laboratory slide preparation, and forensic evidence collection. Critical precautions include single-use only, sterile technique, proper collection method, and biohazard disposal. Essential consumable in all clinical settings.
ATC pH probe (3-in-1)
A ATC pH Probe (3-in-1) is a combination electrochemistry sensor that integrates pH sensing, reference electrode, and automatic temperature compensation (ATC) into a single probe, designed for accurate, simultaneous measurement of pH and temperature in clinical diagnostic, pharmaceutical quality control, and research laboratories . The built-in ATC sensor automatically corrects pH measurements for temperature-dependent variations in electrode slope, ensuring accurate readings across a temperature range of 0-90°C (or 0-100°C for specialized models) .
The probe features an epoxy body for durability and chemical resistance, an Ag/AgCl reference system (gel-filled or refillable), and a glass sensing bulb with a pH range of 0-14 . Available junction types include wick (general purpose), glass fiber (low maintenance), and ceramic (high precision), allowing selection based on sample type and application requirements . Response time is rapid, with stable readings achieved within 30 seconds at 25°C .
For the clinical laboratory scientist and medical technologist, the ATC pH Probe (3-in-1) simplifies pH measurement of biological fluids including serum, plasma, urine, and cerebrospinal fluid—reducing the need for separate temperature probes and minimizing sample handling . For the clinical pathologist, accurate pH measurement supports diagnosis of metabolic acidosis, alkalosis, diabetic ketoacidosis, and renal tubular disorders. For the quality control chemist, the probe provides reliable pH measurement of calibration buffers and QC samples, ensuring that pH meters used for patient sample testing are properly calibrated and functioning within acceptable parameters .
Compatible with pH meters accepting BNC and Mini-DIN/8-pin connectors, the ATC pH Probe (3-in-1) is an essential tool for clinical chemistry laboratories, pathology departments, pharmaceutical QC labs, and research facilities requiring accurate, reproducible pH measurement for patient sample testing, quality control, and diagnostic applications.
Binocular Electric Microscope
A Binocular Electric Microscope is a standard clinical laboratory instrument featuring binocular eyepieces for comfortable viewing and built-in electric illumination (halogen or LED) for routine diagnostic microscopy across microbiology, hematology, histopathology, cytology, urinalysis, and parasitology. Equipped with 4×, 10×, 40× (high dry), and 100× (oil immersion) plan or plan achromatic objectives, 10× widefield eyepieces with diopter adjustment, Abbe condenser with iris diaphragm, mechanical stage with X-Y controls, and coaxial coarse/fine focusing. Magnification range 40× to 1000× with resolution to 0.2-0.3 micrometres. Primary clinical applications include Gram stain interpretation for bacterial identification, manual differential white blood cell counts, red blood cell morphology assessment, malaria parasite detection, urine sediment examination, Pap smear screening, and semen analysis. Essential equipment in every clinical laboratory for visual examination of stained and unstained specimens, providing definitive diagnosis for countless infectious, hematologic, and neoplastic conditions. Binocular design reduces eye strain during prolonged use, while electric illumination ensures consistent, adjustable lighting for optimal specimen visualization.
BioChem FC-120 Automated Chemistry Analyzer
The BioChem FC-120 Automated Chemistry Analyzer is a fully automated, random access benchtop clinical chemistry analyzer designed for small to medium-volume laboratories, community hospitals, district hospitals, and reference laboratories in emerging healthcare markets . Operating at 100 tests per hour with random access capability and STAT priority function, this open reagent system delivers photometric analysis using 8 interference filters (340-670nm) and disposable cuvette technology (90 cuvettes, 9 strips of 10) that eliminates washing maintenance and cross-contamination concerns .
The analyzer features an all-in-one design with built-in 10.4-inch color touchscreen, integrated computer, thermal printer, and 100,000 test result memory . The 42-position sample rotor and 26-position reagent rotor accept primary tubes, secondary tubes, sample cups, and any commercial reagents, with liquid level detection and collision protection for safe, automatic operation . Bi-directional LIS connectivity supports seamless electronic medical record integration .
For the clinical laboratory scientist and pathologist, the BioChem FC-120 delivers accurate measurement of liver function (ALT, AST, ALP, GGT, bilirubin, total protein, albumin), renal function (urea, creatinine, uric acid), lipid profiles (total cholesterol, triglycerides, HDL, LDL, VLDL, apolipoproteins), cardiac biomarkers (CK, CK-MB, LDH, myoglobin), diabetes markers (glucose, HbA1c), inflammatory markers (CRP, RF, ASO, immunoglobulins), iron studies (iron, TIBC, ferritin), electrolytes (calcium, magnesium, phosphorus), and tumor markers (AFP) . For the patient, rapid, accurate chemistry results enable early diagnosis of hepatitis, cirrhosis, chronic kidney disease, diabetes, hyperlipidemia, pancreatitis, myocardial infarction, and inflammatory disorders—guiding appropriate medical therapy and preventing disease progression and complications.
BioChem FC-200 Automated Chemistry Analyzer
The BioChem FC-200 Automated Chemistry Analyzer is a fully automated, random access benchtop clinical chemistry analyzer designed for mid-volume laboratories in emerging healthcare markets including district hospitals, regional reference laboratories, and facilities transitioning from semi-automated methods . Operating at up to 240 tests per hour with random access capability and STAT priority function , this open reagent system delivers photometric analysis using 8 interference filters (340-670nm) and disposable cuvette technology (81 cuvettes, 9 strips of 9) that eliminates washing maintenance and cross-contamination concerns .
The analyzer features 40 sample positions, 40 refrigerated reagent positions with continuous 24-hour cooling , sample volume 3-45µL , reaction volume 180-500µL , and independent mechanical mixing . The optical system includes a 12V 20W halogen lamp with 5mm optical path length, absorbance range 0.0-3.5Abs, and resolution 0.0001Abs . Temperature control maintains 37°C (±0.1°C) stability . Calibration modes include factor, linear (one-point, multi-point), and non-linear (Logistic-Log 4P/5P, Exponential 5P, Polynomial 5P, Parabola, Spline) . Quality control features Levey-Jennings charting with Westgard multi-rules .
The system connects to an external PC (Windows XP or higher) via RS-232 or RS-232-to-USB with bi-directional LIS interface for electronic medical record integration . Languages include English, Spanish, Russian, and Ukrainian . Power requirements are 220VAC, 50/60Hz, 1500VA . The unit measures 810 x 1150 mm (W x H) and weighs 145 kg . Water consumption is ≤3 liters/hour .
For the clinical laboratory scientist and pathologist in district hospitals, the BioChem FC-200 delivers accurate measurement of liver function (ALT, AST, ALP, GGT, bilirubin, total protein, albumin), renal function (urea, creatinine, uric acid), lipid profiles (total cholesterol, triglycerides, HDL, LDL, VLDL), cardiac biomarkers (CK, CK-MB, LDH), diabetes markers (glucose), inflammatory markers (CRP, RF, immunoglobulins), and iron studies (iron, TIBC, ferritin). For the patient, rapid, high-volume chemistry results enable early diagnosis of hepatitis, cirrhosis, chronic kidney disease, diabetes, hyperlipidemia, pancreatitis, and myocardial infarction—guiding appropriate medical therapy and preventing disease progression and complications, particularly in emerging healthcare markets where laboratory automation was previously unavailable .
BioChem SA Semi Automated Chemistry Analyzer
The BioChem SA Semi Automated Chemistry Analyzer is a compact, semi-automated benchtop clinical chemistry system designed for low to medium-volume clinical laboratories, physician office labs (POLs), and small hospital laboratories . The analyzer performs colorimetric and kinetic analysis of patient samples (serum, plasma, whole blood, urine) using endpoint, kinetic, fixed-time, absorbance, monochromatic, and bichromatic assay types .
The optical system features a 6V 10W halogen lamp with 2000-hour lifespan, 7 standard filters (340, 405, 492, 510, 546, 578, 630nm with ±2nm accuracy), and a quartz glass flow cell (32µL, 10mm optical path) with 0.0001Abs resolution and <1.0% precision . The 37°C incubator with 10 round wells maintains temperature stability of ±0.1°C .
The analyzer features a 7 inch color LCD touchscreen interface , 80 user-defined programmable test profiles , internal storage for 100,000 patient results , internal thermal printer, RS-232 connectivity , and Levy-Jennings quality control with automatic statistical analysis . Calibration options include factor, one-point linear, and multi-point linear modes .
For the clinical laboratory scientist and pathologist, the BioChem SA provides reliable, entry-level chemistry testing for liver function (ALT, AST, ALP, bilirubin, total protein, albumin), renal function (BUN, creatinine, uric acid), lipid profiles (cholesterol, triglycerides, HDL, LDL), pancreatic enzymes (amylase, lipase), and glucose . For the patient, accurate chemistry results enable diagnosis of hepatitis, cirrhosis, chronic kidney disease, diabetes, hyperlipidemia, pancreatitis, and cardiovascular disease, guiding appropriate medical therapy and lifestyle interventions.
Biological Microscope
A Biological Microscope is a Class I medical device (optical instrument) designed for examining stained and unstained biological specimens in clinical, research, and educational laboratories. Available in monocular, binocular, or trinocular configurations with magnification from 40× to 1000× (oil immersion) using 4×, 10×, 40×, and 100× achromatic or plan achromatic objectives, 10× widefield eyepieces, Abbe condenser, mechanical stage, and built-in halogen or LED illumination. Features include coaxial coarse/fine focusing, revolving nosepiece, Köhler illumination alignment, and ergonomic design for comfortable use. Primary clinical applications include microbiological examination (Gram stains, acid-fast stains, wet mounts), hematology (differential counts, RBC morphology, platelet estimation), histopathology (tissue sections, H&E, special stains), cytology (Pap smears, FNAs, body fluids), urinalysis (sediment examination), parasitology (malaria, ova, parasites), and fertility (semen analysis). Essential equipment in every clinical laboratory for infectious disease diagnosis, cancer detection, hematological disorder evaluation, and countless other diagnostic applications requiring direct visualization of specimens. Biological microscopes are the foundation of laboratory medicine, enabling pathologists, microbiologists, hematologists, and laboratory scientists to visualize and interpret the cellular and microbial world for patient diagnosis and care.
Biopsy Needles
Biopsy Needles are sterile, single-use precision medical devices designed to obtain tissue or cellular specimens from internal organs, masses, and lesions for histopathological or cytological diagnosis. Available in core biopsy (automatic spring-loaded, semi-automatic, vacuum-assisted, coaxial) and fine needle aspiration configurations, with gauges ranging from 14G-27G and lengths from 6-25 cm. Core biopsy needles obtain intact tissue cores preserving histological architecture; FNA needles aspirate cellular material for cytological evaluation. Specialized variants include bone marrow biopsy needles (Jamshidi, Illinois), echogenic-tip needles for ultrasound guidance, and MRI-compatible needles (nitinol, titanium). Critical safety requirements include strict image guidance for non-palpable lesions, verification of coagulation status, adherence to single-use protocols, and immediate post-procedure monitoring for complications (hemorrhage, pneumothorax, organ injury). An indispensable tool in interventional radiology, oncology, and minimally invasive diagnosis.
Blood Grouping kit
A Blood Grouping Kit is a Class II medical device (FDA-cleared/CE-marked) containing monoclonal antibodies (Anti-A, Anti-B, Anti-D) and control reagents for determining ABO blood group and Rh factor by agglutination method. The kit includes color-coded reagent vials, reaction cards or slides, mixing sticks, lancets, and capillary pipettes. Test time 2-5 minutes (slide method) or 15-30 minutes (tube method). Interpretation based on agglutination pattern: Anti-A positive = group A; Anti-B positive = group B; both positive = group AB; both negative = group O; Anti-D positive = Rh positive; Anti-D negative = Rh negative. Primary clinical applications include pre-transfusion compatibility testing, prenatal and neonatal testing (Rh incompatibility prevention), preoperative blood typing, blood donor screening, and emergency blood typing. Critical safety precautions include refrigerated storage (2-8°C), proper disposal of lancets in sharps containers, universal precautions for blood samples, and confirmation with reverse typing when possible. Essential kit for transfusion medicine, obstetrics, surgery, and emergency care.
Blood ID Centrifuge
The Blood ID Centrifuge is a specialized benchtop centrifuge designed specifically for blood banking and immunohematology applications using gel card or column agglutination technology. It is optimized for centrifuging gel cards used in ABO/Rh typing, antibody screening, cross-matching, direct and indirect antiglobulin tests (Coombs tests), and antibody identification procedures. Features include fixed-angle or swing-out rotors with specialized gel card holders, programmable cycles (speed, time, acceleration/deceleration) for different test protocols, digital display, imbalance detection, and safety lid lock. Capacity typically 6-24 gel cards per run with speeds optimized at 1,000-2,500 RPM for gel card processing. Primary clinical applications include blood typing and cross-matching in transfusion medicine, antibody identification and titer determination, direct and indirect antiglobulin testing, newborn cord blood testing, donor screening, and quality control in immunohematology. Essential equipment for hospital blood banks, donor centers, and immunohematology reference laboratories requiring standardized, reproducible gel card test results.
Blood Lancets
Blood Lancets are sterile, single-use, precision-engineered sharp devices designed to obtain capillary blood specimens via controlled skin puncture (fingerstick, heel stick, or alternate site). Available in standard (21G-28G) and safety (auto-retracting) configurations, with fixed or adjustable penetration depths (0.65 mm - 2.2 mm). Safety lancets with automatic needle retraction are OSHA-mandated for healthcare workers to eliminate sharps injury risk. Specialized variants include ultra-thin (30G-33G) low-pain lancets for frequent testers, pediatric lancets with reduced depth, and neonatal heel stick lancets featuring incision-style blades with strict depth limitation (≤2.0 mm per CLSI). Essential for diabetes self-monitoring, point-of-care testing (glucose, HbA1c, PT/INR, cholesterol), and newborn metabolic screening. Critical safety imperatives include absolute single-use protocol, immediate activation of safety mechanisms or disposal into sharps containers, appropriate depth selection to prevent tissue injury, and rigorous infection control practices. An indispensable medical consumable in chronic disease management, acute care, and preventive medicine.
Bluetooth Blood Pressure Machine With ECG
A Bluetooth Blood Pressure Machine With ECG is an integrated home monitoring device combining automatic oscillometric blood pressure measurement with single-lead ECG recording, featuring Bluetooth connectivity for wireless data transmission to smartphones and healthcare providers. Measures systolic (60-260 mmHg) and diastolic (40-200 mmHg) pressure with ±3 mmHg accuracy (meets AAMI/ESH/ISO standards) and records 30-60 second single-lead ECG with automated detection of atrial fibrillation, bradycardia, and tachycardia. Stores 90-200 readings with date/time stamp; transmits data via Bluetooth 4.0+ to dedicated apps for trend analysis and provider sharing. Primary clinical applications include comprehensive cardiovascular monitoring for hypertensive patients with arrhythmia risk, atrial fibrillation screening during routine BP checks, medication titration monitoring (antihypertensive and antiarrhythmic), preoperative cardiovascular assessment, post-stroke or post-MI secondary prevention, and stress/anxiety monitoring. Class II medical device requiring FDA clearance for both functions. Critical safety considerations include device not for emergency use, ECG screening not equivalent to diagnostic 12-lead, proper cuff placement (bare arm at heart level), ECG signal quality optimization, movement avoidance during measurement, arrhythmia alerts requiring medical follow-up, and regular calibration verification.
Brucella Set
A Brucella Set is a comprehensive serological test system (Class II medical device, CE-marked/FDA-cleared) for qualitative and quantitative detection of antibodies against Brucella species (B. abortus, B. melitensis, B. suis, B. canis) using multiple methodologies including tube agglutination, slide agglutination, and 2-mercaptoethanol (2-ME) testing. The set includes killed, stained Brucella antigens, positive and negative controls, dilution tubes, reaction cards, and 2-ME reagent for IgM/IgG differentiation. Diagnostic titer ≥1:160 or fourfold rise confirms brucellosis. Primary clinical applications include diagnosis of brucellosis in endemic regions (undulant fever, night sweats, arthralgia), fever of unknown origin investigation, occupational health screening in high-risk workers (veterinarians, farmers, slaughterhouse workers), diagnosis of focal complications (sacroiliitis, spondylitis, meningitis, endocarditis), treatment monitoring (fourfold decline indicates response), outbreak investigation, and public health surveillance. Critical safety precautions include handling all samples in biosafety cabinet (Brucella is highly infectious via aerosol), 2-ME reagent toxicity (use fume hood), awareness of prozone phenomenon (serial dilutions essential), cross-reactions with other Gram-negative bacteria, and mandatory reporting to public health authorities. Essential test for brucellosis diagnosis in endemic regions and occupational health settings.
Coagulation Analyzer (TS4000)
The Coagulation Analyzer (TS4000) is a semi-automated, 4-channel benchtop coagulation analyzer using dual magnetic bead (electromechanical) clot detection technology to measure PT (prothrombin time), APTT (activated partial thromboplastin time), TT (thrombin time), and FIB (fibrinogen) in citrated plasma and whole blood samples . With a test range of 3-999 seconds, repeatability of <3% CV, and 4 channels for simultaneous testing , the analyzer delivers rapid, reliable coagulation profiles for preoperative risk assessment, anticoagulant therapy monitoring, and bleeding disorder diagnosis .
The Coagulation Analyzer (TS4000) features a 240×128 dot matrix LCD display, built-in thermal printer, 16 sample pre-warming positions, 5 reagent pre-warming positions (1 with stirring) , open reagent system compatible with any manufacturer's reagents, and electronic linked pipette with auto-start trigger for hands-free operation . Calibration curve storage for up to 18 parameters (5 points each) , 12-month QC data storage for PT, APTT, TT, FIB, RS-232 connectivity for LIS integration, and multi-unit result reporting (sec, %, g/L, mg/dL, IU/mL, %-INR, Ratio, Ratio-INR) ensure laboratory standards compliance .
For the anesthesiologist and hematologist, the Coagulation Analyzer (TS4000) delivers preoperative coagulation screening to identify high-risk surgical bleeding, INR monitoring for warfarin dose titration in atrial fibrillation and mechanical heart valve patients, APTT monitoring for heparin therapy, fibrinogen quantification for DIC diagnosis, and factor assays for inherited bleeding disorders (hemophilia A/B, factor deficiencies) . For the patient, accurate coagulation testing enables early detection of bleeding disorders before surgery, safe anticoagulation to prevent stroke and hemorrhage, diagnosis of DIC in critical illness, and appropriate factor replacement for hemophilia—preventing catastrophic bleeding, thrombotic complications, and improving survival across surgical, cardiac, and emergency care settings.
Combination ORP probe
A Combination ORP Probe is an integrated electrochemistry sensor that combines both the platinum sensing electrode and Ag/AgCl reference electrode into a single probe body, designed for precise measurement of oxidation-reduction potential (ORP) in clinical diagnostic, blood bank, and research laboratory applications . ORP (also known as redox potential) measures the total oxidizing or reducing capability of a biological solution, providing information about the oxidative stress status and electrochemical balance of patient specimens .
The probe features a platinum band sensing element (for ORP measurement) and an Ag/AgCl reference system, with body materials available in epoxy for rugged general-purpose use, glass for chemical resistance in organic solvents, or PPS (polyphenylene sulfide) for super rugged industrial applications . The reference junction options include porous Teflon for general use, Sure-Flow for clogging prevention in dirty or viscous samples, and glass fiber or ceramic for high precision, with single-junction or double-junction designs . Select models (e.g., Triode series) integrate a built-in temperature sensor for automatic temperature compensation (ATC) . Response time is rapid, with stable readings achieved within 10-30 seconds .
For the clinical laboratory scientist and medical technologist, the combination ORP probe simplifies redox measurement of biological fluids including serum, plasma, urine, and blood products—eliminating the need for separate reference and sensing electrodes while reducing sample handling . For the clinical pathologist and researcher, ORP measurement of patient specimens may support the diagnosis, evaluation, and monitoring of conditions including trauma, viral infection, and suspected myocardial infarction, as well as assessment of oxidative stress and systemic inflammation . For the blood bank technologist, ORP measurement of stored blood components can help evaluate quality and storage-related oxidative changes .
Gel-filled (sealed) models require virtually no maintenance as there is no need to refill the reference chamber, while refillable models allow for extended service life . The probe's rugged epoxy body and Sure-Flow junction design is well-suited for dirty or viscous biological samples . Compatible with ORP meters accepting BNC connection, the combination ORP probe is an essential tool for clinical chemistry laboratories, blood banks, transfusion medicine services, and research facilities requiring accurate, reproducible ORP measurement for patient sample testing, quality control, and diagnostic applications .
CRP Test Kit
CRP Test Kit (C-Reactive Protein) is a quantitative or semi-quantitative immunoassay (latex agglutination, turbidimetry, nephelometry, ELISA, or rapid immunochromatographic) for detecting C-reactive protein in blood, an acute-phase reactant produced in response to inflammation. Rapid rise within 6-12 hours, peaks at 24-48 hours, half-life 19 hours. Normal <5-10 mg/L; mild elevation 10-100 mg/L (viral infections, autoimmune flares); moderate 100-200 mg/L (bacterial infections); marked >200 mg/L (sepsis, major trauma). High-sensitivity CRP (hs-CRP) detects 0.1-10 mg/L for cardiovascular risk stratification (<1 mg/L low risk, 1-3 mg/L moderate, >3 mg/L high). Primary clinical applications include detection and monitoring of inflammation, diagnosis and management of infections (differentiating bacterial from viral), assessment of autoimmune disease activity, post-surgical monitoring for complications, cardiovascular risk screening (hs-CRP), monitoring rheumatic fever and inflammatory conditions, and neonatal sepsis evaluation. Critical safety precautions include proper sample handling (universal precautions), quality control verification, awareness of non-specific elevation, prozone phenomenon in very high concentrations, and clinical correlation for interpretation. Essential test for evaluating inflammation across all medical specialties.
E-lyte Plus Advanced Electrolyte Analyzer
The E-lyte Plus Advanced Electrolyte Analyzer is a fully automated, microprocessor-controlled benchtop electrolyte analyzer that uses Ion Selective Electrode (ISE) technology for simultaneous measurement of potassium (K+), sodium (Na+), chloride (Cl-), ionized calcium (Ca++), pH, and lithium (Li+) in whole blood, serum, plasma, and urine samples . With up to six electrodes installed simultaneously, test times of 30-40 seconds, and an optional 21-position autosampler, the system delivers rapid, high-throughput electrolyte profiling in emergency, critical care, and routine laboratory settings .
The system features a 7-inch color LCD touchscreen with user-friendly interface, fast-access menus, and real-time result review . Quality control includes automatic ISE calibration, 3-level QC with Levey-Jennings charting, and automatic QC correction . The analyzer stores 8,000 test results, includes an integrated thermal printer, offers RS-232 connectivity for LIS integration, and supports optional barcode reader for sample ID entry .
For the emergency physician and critical care specialist, the E-lyte Plus provides rapid (30-40 second) sodium, potassium, chloride, and ionized calcium results essential for diagnosing life-threatening electrolyte disturbances—hyponatremia (seizures, coma), hyperkalemia (cardiac arrest), hypocalcemia (tetany, laryngospasm), and acid-base disorders via anion gap calculation. For the psychiatrist, lithium measurement enables therapeutic drug monitoring for bipolar disorder patients, preventing lithium toxicity (tremor, seizures, coma) while ensuring therapeutic efficacy. For the nephrologist and endocrinologist, comprehensive electrolyte panels support diagnosis of adrenal insufficiency (Addison's disease: hyponatremia, hyperkalemia), hyperaldosteronism (Conn's syndrome: hypokalemia), and primary hyperparathyroidism (hypercalcemia). For the patient, accurate, stat electrolyte results guide life-saving interventions—electrolyte replacement for dehydration, insulin and bicarbonate for diabetic ketoacidosis, dialysis for severe hyperkalemia, and calcium and calcitriol for post-thyroidectomy hypocalcemia—preventing fatal arrhythmias, seizures, coma, and respiratory failure.
ECG Machine
An ECG Machine is a Class II medical device that records and displays the electrical activity of the heart through surface electrodes, producing an electrocardiogram for diagnosis of cardiac conditions. Standard diagnostic machines record 12 simultaneous leads (3 limb, 6 precordial, 1 ground) with frequency response 0.05-150 Hz, sampling rate 500-1,000 Hz, and high-resolution (5-10 µV) signal acquisition. Features include color touchscreen display, thermal array printer, computerized interpretation algorithms, internal memory (50-500+ ECGs), and network connectivity for EMR integration. Lead wires (AHA or IEC color coding) connect to disposable adhesive electrodes. Portable models (5-15 kg) with rechargeable batteries enable bedside and mobile use; cart-mounted units provide full diagnostic capability. Primary clinical applications include diagnosis of arrhythmias (AF, VT, bradycardia), detection of myocardial ischemia/infarction (STEMI, NSTEMI), evaluation of chest pain, preoperative cardiac risk assessment, monitoring electrolyte imbalances, assessment of chamber enlargement, and drug effect/toxicity monitoring. Essential diagnostic equipment in emergency departments, cardiology clinics, ICUs, operating rooms, and primary care settings worldwide.
Electric Centrifuge
An Electric Centrifuge is a Class I medical device that uses rapid rotation to separate fluids of different densities, essential in clinical laboratories for processing blood, urine, and other biological specimens. Available in benchtop, refrigerated, microcentrifuge, hematocrit, and high-speed models with fixed-angle, swinging-bucket, or vertical rotors. Speed range 1,000-30,000+ RPM with RCF up to 65,000+ x g. Features include brushless induction motor, digital controls, imbalance detection, lid lock safety, and programmable protocols. Primary clinical applications include separation of serum/plasma for chemistry and hematology testing, urine sediment analysis for microscopy, platelet-rich plasma (PRP) preparation for regenerative medicine, concentration of bacteria for microbiology, cytology fluid analysis, blood banking, and molecular biology sample processing. Critical safety precautions include proper balancing of loads (weight matching), use of sealed rotors for biohazardous samples, regular rotor inspection for corrosion or cracks, never exceeding maximum rated speed, and never opening lid during operation. Essential equipment in clinical, research, and teaching laboratories.
ESR Tubes Glass
ESR Tubes Glass are specialized glass tubes (300 mm length, 2.55 mm bore diameter, graduated 0-200 mm in 1 mm intervals) meeting ICSH and CLSI Westergren specifications for measuring erythrocyte sedimentation rate, a non-specific marker of inflammation. Used with citrated or diluted EDTA blood, filled to exactly 200 mm, placed vertically in Westergren stand, and read at 60 minutes. Primary clinical applications include determination of ESR for diagnosing and monitoring inflammatory conditions (infections, autoimmune disorders, malignancies), monitoring disease activity in rheumatoid arthritis, assessment of temporal arteritis and polymyalgia rheumatica, evaluation of infection and inflammatory response, screening for occult inflammatory conditions, and monitoring chronic inflammatory diseases (SLE, IBD, vasculitis). Critical safety precautions include handling glass tubes carefully to avoid breakage (sharps hazard), proper disposal in sharps containers as biohazardous waste, ensuring vertical alignment and constant temperature (18-25°C), reading at exactly 60 minutes, and avoiding air bubbles and vibration. Essential consumable for reference Westergren ESR testing in clinical laboratories.
Fetal & Maternal Monitor
A Fetal & Maternal Monitor is an electronic monitoring system that simultaneously records fetal heart rate (via external ultrasound or internal scalp electrode), uterine contractions (via external tocodynamometer or intrauterine pressure catheter), and maternal vital signs (blood pressure, heart rate, oxygen saturation). Used for antepartum and intrapartum fetal assessment, non-stress tests, contraction stress tests, and monitoring of high-risk pregnancies including gestational diabetes, hypertensive disorders, and multiple gestations. Features high-resolution display, continuous paper recording, alarm systems for fetal distress, and data storage for medical records. External monitoring is non-invasive for routine use; internal monitoring provides more accurate data but requires ruptured membranes and cervical dilation. Class II medical device requiring FDA clearance and qualified interpretation of fetal heart rate patterns. Essential for assessing fetal well-being and guiding obstetric interventions.
Fetoheart Sonic Aid Doppler (clinic/hospital use)
A Fetoheart Sonic Aid Doppler (Fetal Doppler) is a Class II medical ultrasound device (2-3 MHz probe) for real-time detection and audible/visual display of fetal heart rate in clinical obstetric settings from 10-12 weeks gestation. Features include handheld or tabletop console, waterproof probe, digital heart rate display (30-240 bpm), amplified speaker, headphone jack, and rechargeable battery or AC power operation. Continuous wave or pulsed wave Doppler technology with auto-correlation signal processing rejects maternal artifact. Primary clinical applications include fetal heart rate detection and monitoring during routine prenatal visits, confirmation of fetal viability in first trimester, intermittent fetal monitoring during labor, non-stress test administration, multiple gestation assessment, fetal presentation determination, and post-procedure confirmation (amniocentesis, CVS, ECV). Critical safety considerations include following ALARA principle (minimum necessary exposure), appropriate ultrasound gel use, probe pressure avoidance, infection control (probe cleaning between patients), differentiation of fetal from maternal signals, and interpretation by qualified providers. Essential equipment in outpatient obstetric clinics, hospital labor and delivery units, and prenatal care settings.
Finecare Analyzer
The Finecare Analyzer is a Class II medical device (FDA-cleared, CE-marked) fluorescence immunoassay system manufactured by Wondfo Biotech for quantitative detection of cardiac markers (troponin I, CK-MB, myoglobin), inflammatory markers (CRP, procalcitonin), thyroid hormones (TSH, FT3, FT4), diabetes markers (HbA1c), reproductive hormones (LH, FSH, prolactin), tumor markers (AFP, CEA, PSA), and infectious disease markers. Features include time-resolved fluorescence technology, color touchscreen interface, built-in printer (select models), USB/Ethernet connectivity, and internal rechargeable battery for portable use. Test time 3-15 minutes, sample volume 50-100 µL (whole blood, serum, plasma). Primary clinical applications include rapid diagnosis of acute myocardial infarction in chest pain patients, early detection of sepsis and bacterial infections, thyroid disorder diagnosis and monitoring, long-term glycemic control assessment in diabetes, fertility and reproductive health evaluation, cancer screening and surveillance, and infectious disease testing in endemic and clinical settings. Critical safety precautions include proper test cartridge storage (2-8°C), regular quality control, biohazard safety protocols, and operator training. Essential point-of-care testing system for hospitals, clinics, and remote healthcare facilities requiring rapid, quantitative results.
Flexible Fiber Optic Laryngoscope
A Flexible Fiber Optic Laryngoscope is a flexible endoscope (2-5 mm diameter, 30-60 cm working length) with fiber optic image transmission and steerable tip (120-180° angulation) for visualization of the upper airway and facilitation of difficult intubations. Features include control handle with angulation lever, working channel (1-2 mm) for suction or oxygen, external light source (halogen/xenon/LED), and optional camera for video display. Primary clinical applications include awake intubation in difficult airway management (limited mouth opening, cervical spine instability, obstructing pathology), nasotracheal intubation for oral surgery or maxillofacial trauma, intubation with cervical spine precautions (minimal neck movement), diagnostic airway assessment (stridor, hoarseness, vocal cord dysfunction, masses), double-lumen tube placement for thoracic surgery, pediatric difficult airway management, and tracheostomy tube placement guidance. Class II medical device requiring FDA clearance. Critical safety considerations include mandatory leak testing before immersion, antifog preparation, gentle insertion technique, airway maintenance with oxygen, topical anesthesia for patient comfort, suction availability, backup airway device, and strict infection control with validated reprocessing protocols.
Fluorescent Microscope
A Fluorescent Microscope is a specialized Class I medical device designed for visualizing specimens labeled with fluorescent dyes (fluorochromes) that emit light at specific wavelengths when excited by high-intensity illumination. Equipped with high-pressure mercury (HBO), xenon (XBO), metal halide, or LED light sources, interchangeable filter cubes for specific fluorochromes (DAPI, FITC, TRITC, Cy3, Cy5), and high numerical aperture objectives for maximum light collection. Features include epifluorescence design, precision filter turret (4-6 positions), UV-blocking safety shields, and trinocular head for digital imaging. Primary clinical applications include immunofluorescence for autoimmune disease diagnosis (ANA, ANCA, anti-dsDNA, skin/kidney biopsies), fluorescence in situ hybridization (FISH) for genetic abnormalities (aneuploidy, deletions, translocations, HER2 amplification), auramine-rhodamine staining for tuberculosis screening, direct fluorescent antibody (DFA) testing for Legionella, Pneumocystis, Cryptosporidium, Giardia, and respiratory viruses, and FTA-ABS confirmatory testing for syphilis. Essential equipment in immunology, microbiology, pathology, cytogenetics, and molecular diagnostics laboratories requiring sensitive and specific detection of fluorescent signals for diagnosis of infectious, autoimmune, genetic, and neoplastic diseases.
Glucosics Blood Sugar Sticks
Glucosics Blood Sugar Sticks are single-use, disposable electrochemical test sticks (ISO 15197:2013 compliant) designed exclusively for use with Glucosics glucose meters to measure capillary blood glucose from 0.5-1.0 µL samples in 5-7 seconds. Each stick contains glucose oxidase or glucose dehydrogenase reagents that generate electrical current proportional to glucose concentration (20-600 mg/dL range). Packaging options include multi-stick vials (25-100 sticks) with desiccant for daily use or individually foil-wrapped sticks for travel. Sticks feature no-coding automatic calibration, hematocrit compensation (20-60%), and interference resistance. Primary clinical applications include daily blood glucose testing for Type 1, Type 2, and gestational diabetes management, hypoglycemia and hyperglycemia detection, pre- and post-meal glucose assessment, and hospital point-of-care testing. Critical safety precautions include single-use only, immediate vial closure after stick removal to prevent humidity damage, storage at 2-30°C away from bathrooms and temperature extremes, never using expired sticks, proper hand hygiene before testing, and disposal in sharps containers. Essential consumable for diabetes self-management when used with Glucosics meters.
H. pylori Test Strips
H. pylori Test Strips are rapid, lateral flow immunochromatographic devices used for the qualitative detection of Helicobacter pylori antigens in human stool. As a non-invasive stool antigen test (SAT), it provides a convenient and reliable method for diagnosing active H. pylori infection and confirming eradication after therapy, with results available in under 15 minutes. Ideal for use in clinics and outpatient settings, it aids in the management of dyspepsia and peptic ulcer disease. Proper sample handling, adherence to pre-test medication restrictions, and strict biohazard precautions are essential for obtaining accurate results.
H.pylori test kits (Antigen)
H.pylori test kits (Antigen) are Class II medical devices (FDA-cleared/CE-marked) for rapid immunochromatographic or enzyme immunoassay detection of Helicobacter pylori antigens in stool specimens, enabling non-invasive diagnosis of active infection and post-treatment eradication confirmation. Test principles use monoclonal or polyclonal antibodies specific to H. pylori antigens, producing visible results in 10-20 minutes (rapid tests) or 1-2 hours (EIA). Sensitivity 90-98%, specificity 92-99% compared to gold standard methods. Primary clinical applications include rapid diagnosis of H. pylori infection in patients with dyspepsia, initial screening in uncomplicated dyspepsia (test-and-treat strategy), confirmation of active infection before therapy, post-treatment eradication confirmation (4-6 weeks after therapy), pediatric testing (preferred non-invasive method), screening in high-risk populations (family history of gastric cancer), and monitoring in patients with peptic ulcer disease or MALT lymphoma. Critical safety precautions include mandatory washout period (4 weeks off antibiotics, 2 weeks off PPIs) to avoid false negatives, proper specimen handling (universal precautions), refrigerated storage of kits (2-30°C), quality control verification, and disposal as biohazardous waste. Essential non-invasive tool for H. pylori management in gastroenterology and primary care.
Hemoglobin Meter
A Hemoglobin Meter is a Class II medical device (FDA-cleared, CE-marked) for quantitative point-of-care measurement of hemoglobin concentration in capillary or venous blood, providing results in 5-60 seconds from a 5-20 µL sample. The meter uses photometric, electrochemical, or conductivity technology to measure hemoglobin, with accuracy ±0.3-0.5 g/dL compared to reference methods. Features include backlit LCD display, memory storage for 100-1000 results, USB/Bluetooth connectivity for data transfer, and compatibility with single-use disposable cuvettes or test strips. Primary clinical applications include anemia screening and diagnosis (WHO criteria), preoperative assessment and surgical planning, antenatal care and maternal health monitoring, malaria-endemic region screening, chronic disease management (CKD, IBD, cancer), nutritional assessment and intervention programs, and blood donor screening. Critical safety precautions include single-use lancets, proper hand hygiene, correct sample application, quality control with control solutions, proper cuvette storage (protect from heat, light, humidity), and never using expired cuvettes. Essential point-of-care device for hemoglobin testing in hospitals, clinics, community health programs, and blood donation centers.
Hepatitis B Test Kit
The Hepatitis B Test Kit is an in vitro diagnostic device for the detection of Hepatitis B virus markers in human blood samples, available in rapid, ELISA, and molecular formats. It detects specific antigens (HBsAg) and antibodies (anti-HBc, anti-HBs) to diagnose acute and chronic infection, monitor treatment response, screen blood donations, and determine immunity status. With high sensitivity (>98%) and specificity (>99%), it provides results in 15 minutes to 4 hours depending on format. Essential applications include prenatal screening to prevent mother-to-child transmission, evaluation of acute hepatitis, pre-immunosuppression screening, and occupational health testing. All patient samples must be handled with universal precautions, and testing must include appropriate quality controls.
Hepatitis C Test Kit
The Hepatitis C Test Kit is an in vitro diagnostic device for the detection of Hepatitis C virus antibodies or RNA in human blood, serum, or plasma samples. Available in rapid, laboratory immunoassay, and molecular formats, it screens for HCV infection, confirms active infection with RNA testing, and monitors treatment response. With high sensitivity and specificity exceeding 99%, it is essential for identifying infected individuals, linking them to curative direct-acting antiviral therapy, and confirming cure. Essential applications include risk-based screening of high-risk populations, birth cohort screening of baby boomers, evaluation of acute hepatitis, management of occupational exposures, and monitoring of antiviral therapy that can cure over 95% of infections. All patient samples must be handled with universal precautions, and positive antibody results require confirmatory testing.
Macintosh Bulb Laryngoscope
A Macintosh Bulb Laryngoscope is a rigid laryngoscope with curved Macintosh blade (sizes 0-4, 70-160 mm) featuring a distal incandescent (xenon, krypton, halogen) or LED bulb at the blade tip for direct illumination during tracheal intubation. The curved blade design allows indirect epiglottis elevation by placing the tip in the vallecula, requiring less force and neck extension than straight blades. Features stainless steel reusable blades (or disposable plastic), ergonomic handles with knurled grip, ISO standard hook-on fittings, and autoclavable options. Light output 500-3,000 Lux depending on bulb type and battery condition. Primary clinical applications include routine and emergency tracheal intubation during general anesthesia, difficult airway management, cervical spine precautions (minimal neck movement), rapid sequence intubation, neonatal and pediatric intubation (sizes 0-2), teaching and training, and use in resource-limited settings. Class II medical device requiring FDA clearance. Critical safety considerations include pre-use light check (brightness, bulb security), appropriate blade size selection, proper lifting technique (not levering on teeth), battery verification, bulb obstruction risk from secretions, backup device availability, and infection control (sterilization or disposable blades).
Macintosh Fiber Optic Laryngoscope
A Macintosh Fiber Optic Laryngoscope is a rigid laryngoscope with curved Macintosh blade (sizes 0-4, 70-160 mm) incorporating an integrated fiber optic light bundle that transmits bright, focused illumination (2,000-10,000+ Lux) from a handle-mounted LED or xenon bulb to the blade tip for enhanced visualization during tracheal intubation. The curved blade design allows indirect epiglottis elevation by placing the tip in the vallecula, requiring less force and neck extension than straight blades. Features stainless steel reusable blades, ergonomic handles with knurled grip, ISO standard hook-on fittings, and steam autoclave compatibility. Primary clinical applications include routine and emergency tracheal intubation during general anesthesia, difficult airway management with improved illumination, cervical spine precautions (minimal neck movement), teaching and training (enhanced visualization for instructors), rapid sequence intubation, neonatal and pediatric intubation (sizes 0-2), and oral/maxillofacial surgery. Class II medical device requiring FDA clearance. Critical safety considerations include pre-use light check (dark spots indicate broken fibers), appropriate blade size selection, proper lifting technique (not levering on teeth), battery verification, fiber optic care (avoid sharp bending), and backup device availability.
Manual Centrifuge
A Manual Centrifuge (hand-powered) is a non-electric mechanical device for separating fluids based on density, designed for use in field clinics, remote health posts, and developing world settings where electricity is unavailable or unreliable. Operated by hand crank, pull-cord, or foot pedal, achieving speeds of 1,000-4,000 RPM and RCF up to 1,500 x g. Accepts standard blood collection tubes (2-5 mL), microhematocrit tubes, and small centrifuge tubes. Primary clinical applications include separation of serum/plasma for basic diagnostic testing, urine sediment concentration for microscopy, microhematocrit determination for anemia screening, concentration of parasites for malaria and other vector-borne disease diagnosis, field epidemiology and outbreak investigation, veterinary medicine in rural settings, and teaching in resource-limited institutions. Critical safety precautions include meticulous balancing of tubes by weight (absolutely essential), never exceeding maximum rated speed, using appropriate PPE (no aerosol containment), regular inspection of gears and rotor for wear, and proper training of operators. Essential equipment for basic laboratory capabilities in low-resource and field settings.
MicroCC-20 Plus VET Advanced Hematology Analyzer
The MicroCC-20 Plus VET Advanced Hematology Analyzer is a fully automated, 3-part differential (3-diff) benchtop veterinary hematology analyzer designed for companion animal, livestock, equine, and exotic species CBC testing . The instrument measures 20 parameters including complete blood count (CBC) with WBC, RBC, HGB, HCT, MCV, MCH, MCHC, RDW-SD, RDW-CV, PLT, MPV, PDW, PCT, P-LCR , and a 3-part white blood cell differential (LYM, MID, GRA) with both absolute counts and percentages .
Operating at 60 tests per hour with sample volumes of just 9.8 µL for whole blood or 20 µL for pre-diluted capillary samples , the analyzer uses electrical impedance technology (80 µm ruby aperture) for RBC and platelet counting, and colorimetric photometry (550 nm) for hemoglobin measurement . The 10.4 inch color LCD touchscreen with Windows-based operating system provides an intuitive graphical user interface with language options including English, Russian, Spanish, French, Ukrainian, and Chinese .
Pre-programmed species reference intervals are available for cat, dog, rabbit, pig, goat, horse, cow, buffalo, monkey, and 4 free programmable profiles for other mammals . The analyzer features comprehensive quality control with built-in L‑J, X‑R, and X‑B charting, 50,000 patient result memory with complete histograms and demographics , reagent level monitoring , and connectivity options including RS-232, USB x2, and RJ-45 Ethernet for LIS integration and external peripherals (keyboard, mouse, barcode reader, printer) .
For the veterinarian and veterinary laboratory scientist, the MicroCC‑20 Plus VET provides reliable, cost-effective hematology testing that supports accurate diagnosis of anemia, infection, inflammation, thrombocytopenia, and hematologic disorders across multiple species—including dogs, cats, horses, cattle, swine, goats, rabbits, and non-human primates . For the animal patient, rapid (60 tests/hour) and accurate CBC results enable timely diagnosis of anemia, early detection of infection, monitoring of chemotherapy effects, preoperative risk assessment, and appropriate treatment for bleeding disorders and hematologic diseases—improving veterinary patient outcomes across companion animal, livestock, equine, and wildlife medicine.
MicroCC-25 Plus Advanced Hematology Analyzer
The MicroCC-25 Plus Advanced Hematology Analyzer is a fully automated, 5-part differential (5-diff) benchtop hematology analyzer designed for small to medium-volume clinical laboratories, hospital satellite labs, and physician office laboratories . The instrument measures 25 parameters including complete blood count (CBC) with WBC, RBC, HGB, HCT, MCV, MCH, MCHC, RDW-CV, RDW-SD, PLT, MPV, PDW, PCT, P-LCR, P-LCC , and a five-part white blood cell differential (NEU, LYM, MON, EOS, BAS) with both absolute counts and percentages . It also reports 4 research parameters including atypical lymphocytes (ALY#, ALY%) and immature granulocytes (IG#, IG%) .
Operating at 60 samples per hour with sample volumes of just 15 µL for whole blood or 20 µL for pre-diluted capillary samples , the analyzer uses laser flow cytometry for the 5-part differential, electrical impedance (80 µm ruby aperture) for RBC and platelet counting, and colorimetric photometry (550 nm) for hemoglobin measurement . The 10.4 inch color LCD touchscreen with Windows-based operating system provides an intuitive graphical user interface with language options including English, Spanish, Russian, French, and Ukrainian .
The analyzer features comprehensive quality control with built-in L‑J, X‑R, and X‑B charting, 60 QC files x 500 results, mean/SD/CV% calculation, 100,000 patient result memory with complete histograms and demographics, reagent level monitoring with RFID tag identification, and bi-directional LIS connectivity (HL7 compatible) via USB x4, RJ-45 Ethernet, and external barcode reader . The built-in thermal printer and external printer support provide flexible result output options .
For the clinical laboratory scientist and pathologist, the MicroCC‑25 Plus provides reliable, cost-effective hematology testing that supports accurate diagnosis of anemia, infection, inflammation, thrombocytopenia, and hematologic malignancies across all patient populations including pediatric and geriatric patients requiring minimal specimen volumes . For the patient, rapid (60 tests/hour) and accurate CBC plus 5-part differential results enable timely diagnosis of anemia, early detection of infection, monitoring of chemotherapy effects, preoperative risk assessment, and appropriate treatment for bleeding disorders and hematologic diseases .
Microscope
A microscope is a Class I medical device (optical instrument) essential for visualizing microorganisms, cells, and tissues in clinical diagnostics, featuring magnifications from 40× to 1000× (oil immersion) with brightfield, phase contrast, fluorescence, darkfield, or polarized light capabilities. Standard clinical microscopes are binocular or trinocular with 4×, 10×, 40×, and 100× (oil) plan objectives, 10× widefield eyepieces, Abbe condenser, mechanical stage, and halogen or LED illumination. Fluorescence microscopes add specific filter cubes (FITC, TRITC, DAPI) and high-intensity light sources (mercury/xenon) for FISH, immunofluorescence, and AFB detection. Primary clinical applications include microbiological examination (Gram stains, AFB, wet mounts), hematology (differential counts, RBC morphology), histopathology (tissue sections, H&E, special stains), cytology (Pap smears, FNAs), urinalysis (sediment examination), parasitology (malaria, ova, parasites), and fertility (semen analysis). Essential equipment in every clinical laboratory for infectious disease diagnosis, cancer detection, hematological disorder evaluation, and countless other diagnostic applications requiring direct visualization of specimens.
Miller Fiber Optic Laryngoscope
A Miller Fiber Optic Laryngoscope is a rigid laryngoscope with straight Miller blade (sizes 0-4, 70-160 mm) incorporating an integrated fiber optic light bundle that transmits bright, focused illumination (2,000-10,000+ Lux) from a handle-mounted LED or xenon bulb to the blade tip for enhanced visualization during tracheal intubation. The straight blade design allows direct elevation of the epiglottis rather than the indirect vallecula technique, making it particularly useful for pediatric/neonatal intubation, patients with floppy or prominent epiglottis, anterior airways, and difficult airways requiring direct epiglottic control. Features stainless steel reusable blades, ergonomic handles with knurled grip, ISO standard hook-on fittings, and steam autoclave compatibility. Primary clinical applications include direct epiglottis elevation for tracheal intubation (especially pediatric and neonatal), difficult airway management with fiber optic illumination, patients with prominent or floppy epiglottis, cervical spine precautions, anterior airway management, teaching and training (straight blade technique), and neonatal resuscitation. Class II medical device requiring FDA clearance. Critical safety considerations include pre-use light check (dark spots indicate broken fibers), appropriate blade size selection (especially critical in pediatrics), proper lifting technique (direct epiglottic lift, not levering on teeth), pediatric fragility awareness, battery verification, fiber optic care (avoid sharp bending), and backup device availability.
Mission Plus HB Machine
The Mission Plus HB Machine is a portable, battery-operated hemoglobin meter (Class II medical device, FDA-cleared/CE-marked) using photometric technology to measure hemoglobin concentration in capillary or venous blood within 5-15 seconds. Features include backlit LCD display, memory storage for 100-500 results, simple one-button operation, and disposable single-use cuvettes (5-20 µL sample volume). Accuracy ±0.3 g/dL compared to reference methods, measurement range 4-24 g/dL. Primary clinical applications include rapid anemia screening in outpatient clinics, preoperative assessment, antenatal care and maternal health monitoring, malaria-endemic region screening, chronic disease management (CKD, IBD, cancer), nutritional assessment and intervention programs, and blood donor screening. Critical safety precautions include single-use lancets, proper hand hygiene, correct sample application, quality control with control solutions, proper cuvette storage (protect from heat, light, humidity), and never using expired cuvettes. Essential point-of-care device for hemoglobin testing in diverse healthcare settings.
Mission plus strips
Mission Plus Strips are single-use, disposable electrochemical test strips (ISO 15197:2013 compliant) designed exclusively for use with Mission Plus glucose meters to measure capillary blood glucose from 0.5-1.0 µL samples in 5-7 seconds. Each strip contains glucose oxidase or glucose dehydrogenase reagents that generate electrical current proportional to glucose concentration (20-600 mg/dL range). Packaging options include multi-strip vials (25-100 strips) with desiccant for daily use or individually foil-wrapped strips for travel. Strips feature no-coding automatic calibration, hematocrit compensation (20-60%), and interference resistance. Primary clinical applications include daily blood glucose testing for Type 1, Type 2, and gestational diabetes management, hypoglycemia and hyperglycemia detection, pre- and post-meal glucose assessment, and hospital point-of-care testing. Critical safety precautions include single-use only, immediate vial closure after strip removal to prevent humidity damage, storage at 2-30°C away from bathrooms and temperature extremes, never using expired strips, proper hand hygiene before testing, and disposal in sharps containers. Essential consumable for diabetes self-management when used with Mission Plus meters.
mLabs and qLabs Platforms
The mLabs and qLabs Platforms are integrated point-of-care testing systems manufactured by Micropoint Bioscience for rapid quantitative measurement of coagulation parameters (PT/INR, ACT), cardiac markers (troponin I, CK-MB, NT-proBNP), hemoglobin/hematocrit, electrolytes (Na+, K+, iCa), blood gases (pH, pCO2, pO2), glucose, ketones, and infectious disease markers. The qLabs platform specializes in coagulation and electrolyte testing using electrochemical technology, while the mLabs platform focuses on immunoassay and photometric testing for cardiac, hematology, and infectious disease applications. Features include portable design, touchscreen interface, rechargeable battery, USB/Bluetooth connectivity, and compatibility with single-use disposable test cards. Test times range from 1-15 minutes with sample volumes of 2-100 µL. Primary clinical applications include anticoagulation management (warfarin monitoring), cardiac surgery and intervention support (ACT monitoring), emergency cardiac diagnosis (troponin), anemia screening, diabetes management, critical care electrolyte and blood gas analysis, and infectious disease testing in endemic regions. Critical safety precautions include proper test card storage (temperature-sensitive), regular quality control, operator training, single-use lancets, and infection control protocols. Essential point-of-care testing solution for hospitals, clinics, emergency departments, surgical suites, and anticoagulation clinics.
On Call Blood Sugar Strips
On Call Blood Sugar Strips are single-use, disposable electrochemical test strips (ISO 15197:2013 compliant) designed exclusively for use with On Call glucose meters to measure capillary blood glucose from 0.5-1.0 µL samples in 5-7 seconds. Each strip contains glucose oxidase or glucose dehydrogenase reagents that generate electrical current proportional to glucose concentration (20-600 mg/dL range). Packaging options include multi-strip vials (25-100 strips) with desiccant for daily use or individually foil-wrapped strips for travel. Strips feature no-coding automatic calibration, hematocrit compensation (20-60%), and interference resistance. Primary clinical applications include daily blood glucose testing for Type 1, Type 2, and gestational diabetes management, hypoglycemia and hyperglycemia detection, pre- and post-meal glucose assessment, and hospital point-of-care testing. Critical safety precautions include single-use only, immediate vial closure after strip removal to prevent humidity damage, storage at 2-30°C away from bathrooms and temperature extremes, never using expired strips, proper hand hygiene before testing, and disposal in sharps containers. Essential consumable for diabetes self-management when used with On Call meters.
Pap smear kit
A Pap Smear Kit is a sterile, single-use collection system containing all necessary components for obtaining cervical cell samples for Papanicolaou (Pap) testing and HPV DNA analysis. Each kit typically includes a sterile speculum for cervical visualization, a collection device (cervical broom, endocervical brush, or spatula), and either a liquid-based cytology preservative vial or glass slide with fixative spray. Standardized kits ensure consistent, high-quality specimen collection that maximizes diagnostic accuracy and reduces unsatisfactory sample rates. For the gynecologist and primary care clinician, Pap smear kits provide a convenient, ready-to-use solution that streamlines cervical cancer screening. For the patient, regular Pap screening using standardized kits enables early detection of precancerous cervical changes and high-risk HPV infection—when treatment is most effective—significantly reducing the risk of developing invasive cervical cancer.
Pen torch
A Pen Torch (penlight) is a compact, handheld, battery-powered diagnostic illumination device essential for directed clinical examination including pupillary reflex assessment, oropharyngeal and nasal inspection, wound visualization, foreign body detection, and transillumination. Available in reusable clinical-grade (aluminum/stainless steel, replaceable batteries, LED/incandescent) and disposable (economical plastic, single-patient-use) configurations. LED models provide 20-200 lumens with beam angles 5-60°, color temperature 4000-6500K, and CRI up to 90+ for accurate tissue assessment. Features include pocket clip, end-cap or slide switch, and lightweight construction (20-80 grams). Primary clinical applications include neurological examination (pupillary reflexes, cranial nerve assessment), emergency trauma evaluation, primary care physical examination, critical care monitoring, and pediatric assessment. Class I medical device. Critical safety considerations include ocular safety (avoid prolonged direct exposure), infection control (disinfect reusable devices between patients), battery safety, and contraindication in sterile fields unless sterile-wrapped.
Pinnard Fetoscope (plastic/metal)
A Pinnard Fetoscope (Pinard horn) is a mechanical acoustic horn (150-200 mm length, 40-60 mm bell) for auscultation of fetal heart sounds through the maternal abdomen, available in traditional metal (stainless steel/chrome-plated, 150-300g, autoclavable, durable, requires warming) and modern plastic (medical-grade polymer, 30-80g, lightweight, unbreakable, economical, not autoclavable) versions. The flared bell collects fetal heart sounds, concentrating them through the tapered horn to the single earpiece for mechanical amplification (10-20 dB). Primary clinical applications include intermittent fetal heart rate monitoring during prenatal care and labor in low-risk pregnancies, confirming fetal viability, determining fetal presentation and position through point of maximal intensity, monitoring multiple gestations, and providing non-interventive fetal assessment in natural childbirth, home birth, and resource-limited settings. Class I medical device. Requires significant practitioner training and experience; reliable after 18-20 weeks gestation; limited by maternal obesity, anterior placenta, and ambient noise. Critical safety considerations include infection control (metal autoclavable, plastic chemical disinfection only), gentle abdominal pressure, maternal positioning, and recognition that Pinnard is not a replacement for electronic monitoring in high-risk pregnancies.
Plus Semi-Automated Urine Analyzer (CL-50)
The Plus Semi-Automated Urine Analyzer (CL-50) is a portable, semi-automated urine test strip analyzer that uses LED reflectance photometry (at 550nm, 620nm, and 720nm wavelengths) to measure up to 14 urinary parameters for rapid, objective urinalysis in clinical and point-of-care settings . Throughput is up to 120 tests per hour (continuous mode) or 60 tests per hour (single strip) with a test time of 60 seconds .
The analyzer measures 14 parameters: pH, nitrite, specific gravity, blood (hemoglobin), glucose, bilirubin, urobilinogen, ketones, leukocytes, protein, calcium, creatinine, microalbumin, and ascorbic acid, with automatic result correction eliminating interference from pH, specific gravity, and urine color .
The instrument features an LCD display, built-in thermal printer, internal memory storage for 1,000 test results, connectivity options (RS-232, PS/2, parallel port), optional barcode reader, and automatic calibration for strip sensitivity . Compact (240 x 190 x 115mm) and lightweight (1.3 kg), the CL-50 Plus is briefcase-portable, designed for use in physician office labs, mobile health units, rural health posts, pharmacy screening programs, school health initiatives, and hospital laboratory backup applications .
For the primary care physician and clinical laboratory scientist, the CL-50 Plus enables rapid UTI diagnosis (leukocyte, nitrite detection), diabetes screening (glucose, ketones), preeclampsia detection (protein, microalbumin), chronic kidney disease monitoring (microalbumin, creatinine, ACR), liver disease screening (bilirubin, urobilinogen), and hydration/acid-base assessment (pH, specific gravity). For the patient, rapid, objective urinalysis enables early detection of urinary tract infections (preventing pyelonephritis and sepsis), timely diagnosis of diabetes and preeclampsia (reducing maternal-fetal complications), and early identification of chronic kidney disease (preserving renal function), particularly in underserved communities where traditional laboratory access is limited .
Plus Semi-Automated Urine Analyzer (CL-500)
The Urine Analyzer Plus Semi-Automated (CL-500) is a high-throughput, semi-automated urine test strip analyzer designed for large-volume clinical laboratories, hospital settings, public health screening programs, and high-volume point-of-care facilities . Using LED reflectance photometry at 550nm, 620nm, and 720nm wavelengths, the analyzer measures up to 14 urinary parameters with a throughput of 550 strips per hour and a test time of 65 seconds .
The analyzer features automatic strip feeding for continuous loading without operator intervention, built-in onboard waste collection, and open system compatibility accepting standard urine test strips. The microprocessor-based system stores 5,000 test results with multilingual support (English, Russian, Spanish, Ukrainian), offers comprehensive connectivity (bidirectional LIS, RS-232, USB, WiFi), and includes a built-in thermal printer .
Measured parameters include leukocytes, ketone, nitrite, protein, glucose, blood, calcium, ascorbic acid, urobilinogen, bilirubin, specific gravity, microalbumin, pH, and creatinine—enabling comprehensive urinalysis for UTI diagnosis, diabetes screening, preeclampsia detection, and chronic kidney disease monitoring .
For the clinical laboratory scientist and public health program manager, the CL-500 Plus enables high-volume UTI diagnosis (550 tests/hour), population-based diabetes screening, proteinuria surveillance in large antenatal services, CKD monitoring for hypertension and diabetes programs, and integrated public health reporting via bidirectional LIS connectivity. For the patient, high-throughput urinalysis enables early detection of urinary tract infections (preventing pyelonephritis and urosepsis), timely diagnosis of diabetes and preeclampsia (reducing complications), and early identification of chronic kidney disease (preserving renal function)—particularly in large-scale screening programs where efficient testing is essential for population health impact .
Polypot Container
Polypot Containers are sterile or non-sterile, single-use, leak-proof medical devices manufactured from medical-grade polypropylene for the collection, fixation, transport, and processing of small tissue specimens (biopsies, polyps, surgical excisions) for histopathological examination. Available in capacities ranging from 15 mL to 500 mL, with wide-mouth design for easy specimen deposition and screw-cap closure with tamper-evident seal. Most commonly prefilled with 10% neutral buffered formalin, the standard fixative for routine histology, providing immediate tissue preservation and preventing autolysis. Critical performance attributes include absolute leak-proof integrity to prevent formalin exposure, chemical compatibility with histological reagents, and adequate labeling surface for patient identification. Essential safety principles include strict adherence to formalin hazard precautions (toxic, carcinogenic), immediate specimen labeling at the point of collection to prevent identification errors, and absolute single-use protocol. An indispensable container in surgical pathology, endoscopy, dermatology, and gynecologic procedure settings.
