Snibe MAGLUMI PAP (CLIA)

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Product Details:

Display Type LCD touch screen
Instruments Type Clinical Laboratory Analyzer
Shelf Life N/A (Equipment)
Storage Instructions Keep in a clean, dry environment
Usage Type Laboratory
Accuracy High, within stated clinical limits
Measurement Range As per kit insert for PAP
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Snibe MAGLUMI PAP (CLIA) Price And Quantity

Snibe MAGLUMI PAP (CLIA) Product Specifications

Features High throughput, user-friendly interface, precise results, bar code reader, LIS connectivity
Power Source Electric, AC
Real-Time Operation Yes
Weight Approximately 150 kg
Function Quantitative determination of Prostatic Acid Phosphatase (PAP)
Frequency Depends on sample load
Color White/Blue
Material High-quality medical grade plastic and metal components
Dimension (L*W*H) 910 x 780 x 615 mm
Voltage 220V AC, 50/60Hz
Measurement Range As per kit insert for PAP
Use In-vitro diagnostic testing for PAP (Prostatic Acid Phosphatase)
Power Consumption <1000 VA
Condition New
Technology Chemiluminescence Immunoassay (CLIA)
Accuracy High, within stated clinical limits
Portable No
Equipment Type Immunoassay Analyzer
Instruments Type Clinical Laboratory Analyzer
Operating Type Fully automated
Shelf Life N/A (Equipment)
Storage Instructions Keep in a clean, dry environment
Usage Type Laboratory
Wall Mounted No
Noise Level <60 dB(A)
Display Type LCD touch screen

Quality Control Multi-level QC protocols
Data Storage Large internal memory for results and records
Sample Throughput Up to 180 tests/hour
Calibrator/Control Position Dedicated positions available
Sample Position 60 positions
Warm-up Time <30 minutes
Calibration Automatic, onboard
Interface Options RS232, USB, Ethernet
Barcode Scanner Integrated
Reagent Position Refrigerated, 15 positions
Relative Humidity for Operation 35%-85% (non-condensing)
Ambient Operating Temperature 15°C to 30°C
Sample Type Serum, Plasma

Product Description

Brand	Snibe
Sample Type	Serum
Pack Size	100T
CAT No.	130201006M
Application	Cancer Marker

The kit has been designed for the quantitative determination of Prostatic Acid Phosphatase (PAP) in human serum. The method can be used for samples over the range of 0.5-100 ng/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).

Streamlined High-Throughput Performance

With a capacity of up to 180 tests per hour, the Snibe MAGLUMI PAP (CLIA) significantly boosts laboratory efficiency. The analyzer accommodates up to 60 sample positions, 15 refrigerated reagent slots, and dedicated calibrator/control spots, enabling seamless and continuous operation for busy labs.

Advanced Technology for Accurate Results

Employing chemiluminescence immunoassay (CLIA) technology, this instrument delivers highly accurate and reproducible measurements of Prostatic Acid Phosphatase (PAP). Automatic onboard calibration and multi-level QC protocols further enhance test reliability, meeting clinical diagnostic standards.

User-Friendly Features and Connectivity

A large LCD touch screen paired with integrated barcode scanning ensures intuitive operation. Flexible interface options (RS232, USB, Ethernet) and compatibility with LIS allow smooth data management and connectivity, supporting real-time operation and extensive result storage.

FAQ's of Snibe MAGLUMI PAP (CLIA):

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

A: The analyzer utilizes chemiluminescence immunoassay technology to process serum or plasma samples for quantitative determination of Prostatic Acid Phosphatase (PAP). Its fully automated system handles sample identification, reagent management, calibrator/control application, and result output efficiently.

Q: What is the sample throughput and how does it benefit laboratory operations?

A: The system can process up to 180 tests per hour, enhancing laboratory efficiency by allowing high-volume testing in shorter timeframes. This makes it particularly advantageous for labs with demanding diagnostic workloads.

Q: When is it necessary to calibrate the Snibe MAGLUMI PAP analyzer?

A: Calibration is managed automatically onboard. Calibration frequency is determined by sample load and as recommended in the kit insert, ensuring measurement accuracy and consistency during routine operation.

Q: Where should the Snibe MAGLUMI PAP (CLIA) be installed for optimal operation?

A: It should be placed in a clean, dry laboratory environment with ambient operating temperatures between 15C to 30C and relative humidity of 35%-85% (non-condensing). Proper placement ensures reliable performance and instrument longevity.

Q: What quality control processes are available on this analyzer?

A: The system supports multi-level QC protocols, utilizing dedicated positions for controls. This ensures ongoing verification of result precision and reliability, supporting compliance with clinical laboratory standards.

Q: How can users benefit from the integrated data management and connectivity options?

A: With its internal memory for large-scale result storage and interface options-RS232, USB, and Ethernet-the analyzer seamlessly connects to Laboratory Information Systems (LIS), facilitating efficient workflow, real-time operation, and secure data management.

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