Snibe MAGLUMI C IV (CLIA)

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Product Details:

Shelf Life Not Applicable (Equipment)
Display Type Touchscreen LCD
Function Detection of C IV (Cytomegalovirus IgG/IgM) antibodies
Instruments Type Immunoassay Analyzer
Storage Instructions Store in dry, dust-free environment; avoid direct sunlight
Usage Type Clinical Laboratory Use
Frequency 50/60 Hz
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Snibe MAGLUMI C IV (CLIA) Price And Quantity

Snibe MAGLUMI C IV (CLIA) Product Specifications

Instruments Type Immunoassay Analyzer
Real-Time Operation Yes
Material High-quality Medical Grade Components
Wall Mounted No
Storage Instructions Store in dry, dust-free environment; avoid direct sunlight
Operating Type Automated
Display Type Touchscreen LCD
Shelf Life Not Applicable (Equipment)
Technology CLIA (Chemiluminescence Immunoassay)
Function Detection of C IV (Cytomegalovirus IgG/IgM) antibodies
Condition New
Portable No
Accuracy High accuracy; CV<5%
Power Source Electric
Frequency 50/60 Hz
Measurement Range As per assay kit specification
Weight Approx. 130 kg
Power Consumption 800 VA
Color White/Grey
Features High throughput, automated sample loading, precise detection, user-friendly interface, bar-coded sample identification
Equipment Type Chemiluminescence Immunoassay (CLIA) Analyzer
Voltage 100-240V AC, 50/60Hz
Dimension (L*W*H) 1190 x 590 x 645 mm
Noise Level Low
Use Quantitative detection of C IV antibodies in human serum or plasma
Usage Type Clinical Laboratory Use

Connectivity USB, LAN, LIS integration
Sample Capacity Up to 144 samples per run
Humidity Range 30% to 85% RH, non-condensing
Throughput Up to 180 tests/hour
Environment Operating Temperature 15°C to 30°C
Sample Type Serum, Plasma
Incubation Time Varies as per assay kit (typically 30-45 minutes)
Reagent Capacity 25 reagent positions
Calibration Automatic, bar-code recognized
Printer Interface Built-in or external printer supported

Product Description

Brand	Snibe
Sample Type	Serum
Pack Size	100T
CAT No.	130209003M
Application	Cardiac Marker

The kit has been designed for the quantitative determination of Type IV collagen (C IV) in human serum. The method can be used for samples over the range of 5.0-2000ng/ml. The test has to be performed on the Fully-auto chemiluminescence immunoassay (CLIA) analyzer MAGLUMI (Including Maglumi 600,Maglumi 1000,Maglumi 1000 Plus, Maglumi 2000,Maglumi 2000 Plus,Maglumi 3000 and Maglumi 4000).

Precision and Efficiency in Immunoassay Testing

Engineered for clinical laboratories, the MAGLUMI C IV (CLIA) delivers highly precise results, processing up to 180 samples per hour. Automated calibration and barcoded sample management ensure consistent accuracy and minimal manual intervention. High throughput and multiple reagent positions enhance workflow efficiency, catering effortlessly to busy diagnostic environments.

Advanced Connectivity and User-Friendly Operation

With integrated USB, LAN, and LIS compatibility, data transfer and reporting are seamless. The interactive touchscreen LCD makes navigating operations and monitoring progress intuitive. Offering both built-in and external printer support, the system streamlines result documentation and laboratory workflow.

Designed for Reliability and Ease of Maintenance

Constructed from medical-grade components, the MAGLUMI C IV withstands demanding laboratory conditions. Maintenance is straightforward, thanks to dust-free storage requirements and robust build quality. Its automated functions minimize downtime, ensuring reliable operation and consistent performance every day.

FAQ's of Snibe MAGLUMI C IV (CLIA):

Q: How does the Snibe MAGLUMI C IV (CLIA) analyzer process samples?

A: The analyzer utilizes chemiluminescence immunoassay (CLIA) technology to quantitatively detect C IV (Cytomegalovirus IgG/IgM) antibodies in serum or plasma. It automates sample loading, barcode identification, incubation, reagent handling, and detection to deliver rapid, precise test results.

Q: What environments and storage conditions are suitable for optimal analyzer performance?

A: The MAGLUMI C IV operates best between 15C to 30C with a humidity range of 30% to 85% RH, non-condensing. Store the equipment in a dry, dust-free setting, away from direct sunlight to maintain its longevity and accuracy.

Q: When is calibration required and how is it managed?

A: Calibration is automated and managed by the device via barcode-recognized calibration protocols as specified by the assay kits. This reduces manual workload and ensures consistent accuracy with every batch of tests.

Q: Where can the MAGLUMI C IV be integrated within laboratory workflows?

A: The analyzer is designed primarily for clinical diagnostic laboratories. With its LIS connectivity and multiple data transfer options (USB, LAN), it seamlessly integrates with existing laboratory information systems and workflow setups.

Q: What is the process for running a test on this instrument?

A: Load samples and reagents, and scan barcodes; the analyzer automatically recognizes each sample, initiates incubation (typically 30-45 minutes), and proceeds with measurement. Results are processed in real-time and can be printed or transferred digitally.

Q: How does this analyzer benefit clinical laboratories in India?

A: Featuring high throughput, automated operation, and precise quantitative detection, the analyzer enables laboratories to efficiently manage high sample volumes with reliable results. This enhances diagnostic capacity and workflow efficiency, essential for large-scale screening and monitoring.

Q: What are the usage advantages of the MAGLUMI C IV (CLIA) analyzer?

A: Key advantages include low noise, high accuracy (CV<5%), automated calibration, and a user-friendly touchscreen interface. Its robust construction, real-time operation, and LIS integration support reliable, streamlined laboratory testing.

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