BioChem FC-120 Automated Chemistry Analyzer

WhatsApp Order

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.

Compare

Add to wishlist

Categories: DIAGNOSTIC EQUIPMENT, Diagnostic Kits, Vital Signs Monitors Tags: Automated Chemistry Analyzer, BioChem FC-120, Cardiac Biomarkers, Clinical Chemistry Analyzer, Community Hospital Laboratory, Disposable Cuvette Technology, District Hospital Diagnostics, HTI BioChem FC-120, Lipid Profile, Liver Function Testing, Open Reagent System, Random Access Analyzer, Renal Function Testing, STAT Chemistry

Description

BioChem FC-120 Automated Chemistry Analyzer

PRIMARY CLINICAL & DIAGNOSTIC USES

1. Liver Function Testing (LFT) for Hepatic Disease Diagnosis

Primary Use: Provides a fully automated, random access benchtop chemistry analyzer with 100 tests per hour throughput, performing endpoint, two-point, and kinetic analysis of liver function parameters including ALT, AST, ALP, GGT, total bilirubin, direct bilirubin, total protein, and albumin using 8 standard wavelengths (340-670nm) .
How it helps: For the clinical laboratory scientist and hepatologist, the BioChem FC-120 delivers accurate measurement of hepatic enzymes and bilirubin using photometric optical technology with a 20W halogen lamp and interference filters . For the patient with suspected hepatitis, cirrhosis, fatty liver disease, or drug-induced liver injury, precise liver enzyme quantification enables early diagnosis, monitoring of disease progression, and assessment of treatment response, guiding appropriate hepatology referral and management.

2. Renal Function Testing for Chronic Kidney Disease Management

Primary Use: Measures renal function parameters including urea, creatinine, uric acid, and electrolytes using pre-programmed applications for all HTI reagents . Disposable cuvette technology (90 cuvettes, 9 strips of 10) eliminates washing maintenance and cross-contamination concerns .
How it helps: For the nephrologist and primary care physician, the BioChem FC-120’s random access capability and STAT priority function enable urgent creatinine and urea testing for emergency department patients . For the patient with chronic kidney disease, diabetes, hypertension, or acute kidney injury, accurate renal function testing supports staging of CKD, monitoring of dialysis adequacy, and early detection of nephrotoxicity from medications, enabling timely intervention to preserve renal function.

3. Lipid Profile Testing for Cardiovascular Risk Assessment

Primary Use: Performs comprehensive lipid panel analysis including total cholesterol, triglycerides, HDL cholesterol, LDL cholesterol, VLDL cholesterol, apolipoproteins A1, B, CII, CIII, and E for complete cardiovascular risk stratification . Supports lipoprotein and beta-2-microglobulin testing for advanced cardiac risk assessment .
How it helps: For the cardiologist and preventive medicine specialist, the BioChem FC-120’s simple, intuitive software with pre-loaded applications for all reagents enables lipid profiling for cardiovascular risk stratification . For the patient with hyperlipidemia, diabetes, metabolic syndrome, or established cardiovascular disease, accurate lipid profiling enables calculation of ASCVD risk scores, monitoring of statin therapy effectiveness, and lifestyle modification guidance to reduce myocardial infarction and stroke risk.

4. Comprehensive Enzyme and Substrate Testing for Multiple Clinical Indications

Primary Use: Performs up to 60 different assays including pancreatic enzymes (amylase, lipase), cardiac markers (CK, CK-MB, LDH), electrolytes (iron, calcium, magnesium, potassium, sodium, phosphorus, chlorine, zinc, copper), and therapeutic drug monitoring . Open reagent system with 26 reagent positions and 9 sample positions providing flexible test menu configuration .
How it helps: For the emergency physician, endocrinologist, and clinical chemist, the BioChem FC-120’s random access capability and STAT priority function enable urgent amylase testing for pancreatitis, troponin for myocardial infarction, and glucose for diabetic emergencies . For the patient presenting with acute abdominal pain, chest pain, or altered mental status, rapid enzyme and substrate quantification enables emergency diagnosis of pancreatitis, myocardial infarction, diabetic ketoacidosis, and electrolyte disorders—facilitating appropriate acute care and preventing life-threatening complications .

SECONDARY & SUPPORTIVE USES

1. Diabetes Screening and Glycemic Control Monitoring: Measures glucose and glycated hemoglobin (HbA1c) for diabetes diagnosis, prediabetes screening, and long-term glycemic control monitoring in diabetic patients on insulin or oral hypoglycemic agents .

2. Inflammatory and Autoimmune Disease Assessment: Quantifies C-reactive protein (CRP), rheumatoid factor (RF), anti-streptolysin O (ASO), immunoglobulins (IgG, IgA, IgM), and complement proteins for inflammatory and autoimmune disease diagnosis and activity monitoring .

3. Anemia Workup and Iron Studies: Measures serum iron, total iron-binding capacity (TIBC), ferritin, transferrin, and vitamin B12 for comprehensive iron deficiency anemia and hemochromatosis diagnosis .

4. Bone and Mineral Metabolism Testing: Quantifies calcium, phosphorus, alkaline phosphatase (ALP), and magnesium for osteoporosis, hyperparathyroidism, and metabolic bone disease diagnosis .

5. Tumor Marker Screening: Supports alpha-fetoprotein (AFP) and ferritin testing for hepatocellular carcinoma and other malignancy screening .

6. Therapeutic Drug Monitoring (TDM): Quantifies drug levels for medications with narrow therapeutic indices using the open reagent system and programmable assay parameters.

7. Small and Medium Volume Laboratory Testing: Processes 50-100 samples daily in community hospitals, district hospitals, reference laboratories, and clinic laboratories with low to moderate test volumes .

8. Emergency and STAT Testing: Provides STAT priority function for urgent clinical decisions; STAT samples interrupt routine testing and produce results fast for emergency department patients .

9. Point-of-Care and Physician Office Laboratory (POL) Testing: Compact benchtop design (640x480x510mm, 45kg) with 10.4-inch touchscreen enables decentralized testing in physician offices, urgent care centers, and clinic laboratories .

10. Electronic Medical Record Integration: Bi-directional LIS connectivity streamlines sample tracking, result reporting, and integration with hospital information systems .

11. Quality Control and Laboratory Accreditation: Built-in Levey-Jennings charting with Westgard rules, 100,000 result memory, and comprehensive QC reporting supports laboratory quality assurance programs and ISO accreditation .

12. Cardiac Biomarker Testing: Measures troponin, CK-MB, and myoglobin for acute coronary syndrome diagnosis in emergency department patients .

13. HIV/AIDS Disease Progression Monitoring: Supports immunoglobulin and total protein testing for immune status assessment in HIV patients.

14. Veterinary Diagnostic Applications: Supports biochemistry testing for companion animals, livestock, and research animals .

15. Teaching and Training Laboratory Use: Pre-loaded applications and intuitive touchscreen interface serve as educational instrument for clinical chemistry training.

KEY PRODUCT FEATURES

1. BASIC IDENTIFICATION ATTRIBUTES

Device Type: A fully automated, random access benchtop clinical chemistry analyzer (automatic biochemical analyzer) with STAT capability, open reagent system, and disposable cuvette technology .
Designation: BioChem FC-120 Automated Chemistry Analyzer, HTI BioChem FC-120, Automatic Biochemical Analyzer, Random Access Chemistry Analyzer .
Key Components:

Optical System: 20W halogen lamp with 8 interference filters at wavelengths 340, 405, 450, 510, 546, 578, 630, 670nm; optical path length 5mm .
Sampling System: Automatic probe with liquid level detection, collision protection, high-pressure internal and external washing, automatic liquid aspiration depth adjustment .
Reagent Rotor: 26 positions for reagents (up to 40mL capacity) .
Sample Rotor: 42 positions for samples (primary/secondary tubes, sample cups); 9 standard positions .
Reaction Carousel: 90 disposable cuvettes (9 strips of 10 cuvettes); reaction volume 180-600μL .
Incubator: Temperature control at 37°C, room temperature, or 30°C with ±0.1°C stability .
User Interface: 10.4-inch color touchscreen with intuitive software; pre-loaded applications for all HTI reagents .
Printer: Integrated thermal printer; external printer support .
Computer: Built-in PC with Windows-based operating system .
Memory: 100,000 result storage capacity .
Connectivity: Bi-directional LIS interface, RS-232 .

2. TECHNICAL & PERFORMANCE PROPERTIES

Methodology: Photometric, turbidimetric; endpoint, two-point, and kinetic analysis modes .
Throughput: 100 tests per hour (continuous operation) .
Operating Mode: Random access (discretionary access) allowing any test on any sample without batching .
Sample Types: Serum, plasma, whole blood, urine, cerebrospinal fluid .
Sample Volume: 3-45 μL in 0.1 μL increments .
Reagent Volume: 30-450 μL in 1 μL increments .
Reaction Volume: 180-600 μL .
Optical Path Length: 5 mm .
Absorbance Range: 0.01 to 3.50 B .
Absorbance Precision: ≤0.01 B (0.01-0.5 B range); ≤3.0% relative (0.5-3.5 B range) .
Wavelengths (8 filters): 340, 405, 450, 510, 546, 578, 630, 670nm .
Incubation Temperature: 37°C (±0.1°C), room temperature, 30°C .
Sample Rotor Capacity: 42 positions (up to 5 virtual disks) .
Reagent Rotor Capacity: 26 positions (up to 1 virtual disk) .
STAT Capability: Yes; STAT samples interrupt routine testing for emergency processing .
Calibration Modes: Factor, linear (one-point, two-point, multi-point), nonlinear (Logistic-Log 4P/5P, Exponential 5P, Polynomial 5P, Parabola, Spline) .
Quality Control: Levey-Jennings charting with Westgard rules; internal and external QC .
Result Memory: 100,000 patient results .
Power Requirements: 100-240V, 50/60Hz; 350VA maximum consumption .
Dimensions (W x D x H): 640 x 480 x 510 mm .
Weight: 45 kg .
Operating Temperature: 20-30°C .
Operating Humidity: ≤85% non-condensing .
Water Supply: Built-in container for deionized water with sensor and tubing; waste container with sensor .

3. PHYSICAL & OPERATIONAL PROPERTIES

Construction: All-in-one benchtop design with integrated computer, printer, and touchscreen; durable construction for daily laboratory use .
User Interface: 10.4-inch large color touchscreen with intuitive graphical interface; pre-loaded applications for all HTI reagents; simple enough that users can run samples right out of the box .
Sample Handling: 42-position sample rotor accepts primary tubes, secondary tubes, and sample cups; automatic liquid level detection prevents probe damage .
Reagent Handling: 26-position reagent rotor with liquid level detection; open reagent system compatible with any commercial reagents .
Reaction System: 90 disposable cuvettes (9 strips of 10) on reaction carousel; single-use eliminates washing maintenance and cross-contamination concerns .
Probe System: Automatic sample probe with collision protection (even in external situations), high-pressure internal and external washing, automatic aspiration depth adjustment .
STAT Function: STAT samples get priority automatically; urgent glucose for diabetic crisis, creatinine for pre-surgical clearance, troponin for chest pain in emergency department .
Maintenance: Disposable cuvettes eliminate cuvette washing; self-diagnostic systems and alarms ensure error-free operation .
Calibration: Automatic and manual calibration modes; factory calibration verification recommended annually.
Data Management: 100,000 result memory with patient demographics and QC data; results can be printed via integrated thermal printer or exported via LIS .
Connectivity: Bi-directional LIS interface for seamless integration with laboratory information systems; RS-232 serial port .
Self-Diagnostics: Systems continuously monitor instrument status and alert operator to potential issues .

4. SAFETY & COMPLIANCE ATTRIBUTES

Regulatory Status: In Vitro Diagnostic (IVD) medical device; registered in State Register No. 66945-17; verification interval 1 year .
Safety Certifications: CE marked; compliant with applicable international safety standards.
Infection Control: Disposable cuvettes eliminate cross-contamination risk; automatic probe washing reduces biohazard exposure; closed-tube sampling standard precautions .
Electrical Safety: Wide voltage compatibility (100-240V, 50/60Hz) for international use; Class I protection requiring grounded outlet; 350VA power consumption .
Operating Environment: Designed for indoor laboratory use at 20-30°C temperature, ≤85% humidity .
Quality Assurance: Built-in Levey-Jennings charting with Westgard rules; internal and external QC; self-diagnostic systems .
LIS Compliance: Bi-directional LIS connectivity for electronic result reporting and sample tracking .

5. STORAGE & HANDLING ATTRIBUTES

Storage: Store in clean, dry laboratory environment with temperature 20-30°C. Protect from dust, vibration, and direct sunlight.
Cleaning: Probe self-washing system (high-pressure internal and external). Wipe exterior with soft, damp cloth using mild detergent. Disinfect per facility protocols .
Replacement Parts: Consumables include disposable cuvettes (90 per run, 9 strips of 10), reagent containers (26 positions, 20-40mL capacity), sample tubes, halogen lamp (12V, 20W), 10A fuse .
Water Supply: Requires deionized or distilled water; built-in water container with sensor and tubing .
Waste Management: Built-in waste container with sensor; dispose per facility biohazard protocols .
Maintenance: 1-year verification interval; annual calibration verification recommended; factory-authorized service .
Installation: Benchtop installation requires 64 x 48 cm footprint plus clear access to sides and rear; 45kg weight ensures stable placement; requires nearby electrical outlet (100-240V, 50/60Hz); LIS connectivity via RS-232 recommended for result export.

6. LABORATORY & CLINICAL APPLICATIONS

Primary Application: Fully automated, random access clinical chemistry testing for liver function, renal function, lipid profiling, diabetes monitoring, cardiac biomarkers, and therapeutic drug monitoring in community hospitals, district hospitals, reference laboratories, and clinic laboratories .
Clinical Role: Essential diagnostic instrumentation for primary care, internal medicine, hepatology, nephrology, cardiology, endocrinology, emergency medicine, and infectious disease in emerging healthcare markets .

SAFETY HANDLING PRECAUTIONS

1. SAFETY PRECAUTIONS

Biohazard Exposure: Treat all samples (serum, plasma, urine, CSF) as potentially infectious; use standard precautions (gloves, lab coat, eye protection); dispose of waste per facility biohazard protocol.
Electrical Safety: Use a properly grounded outlet; wide voltage tolerance (100-240V, 50/60Hz) ensures safe international use; disconnect power before maintenance .
Reagent Handling: Use reagents as directed; open system compatible with any commercial reagents; follow SDS for each reagent; avoid skin and eye contact.
Sample Handling: Centrifuge samples per manufacturer guidelines; avoid hemolyzed, lipemic, or icteric specimens which may affect photometric readings.
Quality Control: Run QC materials per laboratory schedule; verify calibration before patient testing; do not report results if QC fails; follow Westgard rules .
Environmental Conditions: Operate within specified temperature (20-30°C) and humidity (≤85%) ranges for optimal photometric performance .
Disposable Cuvettes: Use only supplied cuvettes (90 per run, 9 strips of 10); do not reuse cuvettes .
Training: Only trained laboratory personnel should operate the BioChem FC-120 for clinical diagnostic applications.

2. FIRST AID MEASURES

Sample Exposure: Wash exposed skin immediately with soap and water; flush eyes with water for 15 minutes; follow institutional exposure management protocol.
Reagent Spill: Ventilate area; use absorbent materials; dispose as chemical waste per SDS.
Electrical Malfunction: Disconnect power immediately; do not attempt repair; contact authorized service provider.
QC Failure: If QC fails, repeat QC; if repeated failure, recalibrate; if persistent failure, contact technical support; do not report patient results until QC passes.

3. FIRE FIGHTING MEASURES

Flammability: Electrical hazard; reagents may be combustible.
Extinguishing Media: Use CO₂ or dry chemical extinguisher for electrical fires.
Fire Response: Disconnect power; use appropriate extinguisher; do not use water on electrical fire.

BioChem FC-120 Automated Chemistry Analyzer

BioChem FC-120 Automated Chemistry Analyzer

PRIMARY CLINICAL & DIAGNOSTIC USES

1. Liver Function Testing (LFT) for Hepatic Disease Diagnosis

2. Renal Function Testing for Chronic Kidney Disease Management

Primary Use: Measures renal function parameters including urea, creatinine, uric acid, and electrolytes using pre-programmed applications for all HTI reagents . Disposable cuvette technology (90 cuvettes, 9 strips of 10) eliminates washing maintenance and cross-contamination concerns .

3. Lipid Profile Testing for Cardiovascular Risk Assessment

4. Comprehensive Enzyme and Substrate Testing for Multiple Clinical Indications

SECONDARY & SUPPORTIVE USES

1. Diabetes Screening and Glycemic Control Monitoring: Measures glucose and glycated hemoglobin (HbA1c) for diabetes diagnosis, prediabetes screening, and long-term glycemic control monitoring in diabetic patients on insulin or oral hypoglycemic agents .

2. Inflammatory and Autoimmune Disease Assessment: Quantifies C-reactive protein (CRP), rheumatoid factor (RF), anti-streptolysin O (ASO), immunoglobulins (IgG, IgA, IgM), and complement proteins for inflammatory and autoimmune disease diagnosis and activity monitoring .

3. Anemia Workup and Iron Studies: Measures serum iron, total iron-binding capacity (TIBC), ferritin, transferrin, and vitamin B12 for comprehensive iron deficiency anemia and hemochromatosis diagnosis .

4. Bone and Mineral Metabolism Testing: Quantifies calcium, phosphorus, alkaline phosphatase (ALP), and magnesium for osteoporosis, hyperparathyroidism, and metabolic bone disease diagnosis .

5. Tumor Marker Screening: Supports alpha-fetoprotein (AFP) and ferritin testing for hepatocellular carcinoma and other malignancy screening .

6. Therapeutic Drug Monitoring (TDM): Quantifies drug levels for medications with narrow therapeutic indices using the open reagent system and programmable assay parameters.

7. Small and Medium Volume Laboratory Testing: Processes 50-100 samples daily in community hospitals, district hospitals, reference laboratories, and clinic laboratories with low to moderate test volumes .

8. Emergency and STAT Testing: Provides STAT priority function for urgent clinical decisions; STAT samples interrupt routine testing and produce results fast for emergency department patients .

9. Point-of-Care and Physician Office Laboratory (POL) Testing: Compact benchtop design (640x480x510mm, 45kg) with 10.4-inch touchscreen enables decentralized testing in physician offices, urgent care centers, and clinic laboratories .

10. Electronic Medical Record Integration: Bi-directional LIS connectivity streamlines sample tracking, result reporting, and integration with hospital information systems .

11. Quality Control and Laboratory Accreditation: Built-in Levey-Jennings charting with Westgard rules, 100,000 result memory, and comprehensive QC reporting supports laboratory quality assurance programs and ISO accreditation .

12. Cardiac Biomarker Testing: Measures troponin, CK-MB, and myoglobin for acute coronary syndrome diagnosis in emergency department patients .

13. HIV/AIDS Disease Progression Monitoring: Supports immunoglobulin and total protein testing for immune status assessment in HIV patients.

14. Veterinary Diagnostic Applications: Supports biochemistry testing for companion animals, livestock, and research animals .

15. Teaching and Training Laboratory Use: Pre-loaded applications and intuitive touchscreen interface serve as educational instrument for clinical chemistry training.

1. BASIC IDENTIFICATION ATTRIBUTES

Device Type: A fully automated, random access benchtop clinical chemistry analyzer (automatic biochemical analyzer) with STAT capability, open reagent system, and disposable cuvette technology .

Designation: BioChem FC-120 Automated Chemistry Analyzer, HTI BioChem FC-120, Automatic Biochemical Analyzer, Random Access Chemistry Analyzer .

Key Components:

Optical System: 20W halogen lamp with 8 interference filters at wavelengths 340, 405, 450, 510, 546, 578, 630, 670nm; optical path length 5mm .

Sampling System: Automatic probe with liquid level detection, collision protection, high-pressure internal and external washing, automatic liquid aspiration depth adjustment .

Reagent Rotor: 26 positions for reagents (up to 40mL capacity) .

Sample Rotor: 42 positions for samples (primary/secondary tubes, sample cups); 9 standard positions .

Reaction Carousel: 90 disposable cuvettes (9 strips of 10 cuvettes); reaction volume 180-600μL .

Incubator: Temperature control at 37°C, room temperature, or 30°C with ±0.1°C stability .

User Interface: 10.4-inch color touchscreen with intuitive software; pre-loaded applications for all HTI reagents .

Printer: Integrated thermal printer; external printer support .

Computer: Built-in PC with Windows-based operating system .

Memory: 100,000 result storage capacity .

Connectivity: Bi-directional LIS interface, RS-232 .

2. TECHNICAL & PERFORMANCE PROPERTIES

Methodology: Photometric, turbidimetric; endpoint, two-point, and kinetic analysis modes .

Throughput: 100 tests per hour (continuous operation) .

Operating Mode: Random access (discretionary access) allowing any test on any sample without batching .

Sample Types: Serum, plasma, whole blood, urine, cerebrospinal fluid .

Sample Volume: 3-45 μL in 0.1 μL increments .

Reagent Volume: 30-450 μL in 1 μL increments .

Reaction Volume: 180-600 μL .

Optical Path Length: 5 mm .

Absorbance Range: 0.01 to 3.50 B .

Absorbance Precision: ≤0.01 B (0.01-0.5 B range); ≤3.0% relative (0.5-3.5 B range) .

Wavelengths (8 filters): 340, 405, 450, 510, 546, 578, 630, 670nm .

Incubation Temperature: 37°C (±0.1°C), room temperature, 30°C .

Sample Rotor Capacity: 42 positions (up to 5 virtual disks) .

Reagent Rotor Capacity: 26 positions (up to 1 virtual disk) .

STAT Capability: Yes; STAT samples interrupt routine testing for emergency processing .

Calibration Modes: Factor, linear (one-point, two-point, multi-point), nonlinear (Logistic-Log 4P/5P, Exponential 5P, Polynomial 5P, Parabola, Spline) .

Quality Control: Levey-Jennings charting with Westgard rules; internal and external QC .

Result Memory: 100,000 patient results .

Power Requirements: 100-240V, 50/60Hz; 350VA maximum consumption .

Dimensions (W x D x H): 640 x 480 x 510 mm .

Weight: 45 kg .

Operating Temperature: 20-30°C .

Operating Humidity: ≤85% non-condensing .

Water Supply: Built-in container for deionized water with sensor and tubing; waste container with sensor .

3. PHYSICAL & OPERATIONAL PROPERTIES

Construction: All-in-one benchtop design with integrated computer, printer, and touchscreen; durable construction for daily laboratory use .

User Interface: 10.4-inch large color touchscreen with intuitive graphical interface; pre-loaded applications for all HTI reagents; simple enough that users can run samples right out of the box .

Sample Handling: 42-position sample rotor accepts primary tubes, secondary tubes, and sample cups; automatic liquid level detection prevents probe damage .

Reagent Handling: 26-position reagent rotor with liquid level detection; open reagent system compatible with any commercial reagents .

Reaction System: 90 disposable cuvettes (9 strips of 10) on reaction carousel; single-use eliminates washing maintenance and cross-contamination concerns .

Probe System: Automatic sample probe with collision protection (even in external situations), high-pressure internal and external washing, automatic aspiration depth adjustment .

STAT Function: STAT samples get priority automatically; urgent glucose for diabetic crisis, creatinine for pre-surgical clearance, troponin for chest pain in emergency department .

Maintenance: Disposable cuvettes eliminate cuvette washing; self-diagnostic systems and alarms ensure error-free operation .

Calibration: Automatic and manual calibration modes; factory calibration verification recommended annually.

Data Management: 100,000 result memory with patient demographics and QC data; results can be printed via integrated thermal printer or exported via LIS .

Connectivity: Bi-directional LIS interface for seamless integration with laboratory information systems; RS-232 serial port .

Self-Diagnostics: Systems continuously monitor instrument status and alert operator to potential issues .

4. SAFETY & COMPLIANCE ATTRIBUTES

Regulatory Status: In Vitro Diagnostic (IVD) medical device; registered in State Register No. 66945-17; verification interval 1 year .

Safety Certifications: CE marked; compliant with applicable international safety standards.