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Boditech AFIAS Infliximab Boditech AFIAS Infliximab Boditech AFIAS Infliximab
Boditech AFIAS Infliximab
Boditech AFIAS Infliximab Boditech AFIAS Infliximab

Boditech AFIAS Infliximab

Product Details:

  • Frequency Analyzer-dependent
  • Measurement Range According to kit insert & analyzer
  • Display Type Analyzer-dependent
  • Function Quantitative determination of infliximab levels
  • Features Single-use, quantitative, rapid, reliable, easy handling
  • Shelf Life As per manufacturer: typically up to 12 months
  • Usage Type Laboratory in-vitro diagnostics
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Boditech AFIAS Infliximab Price And Quantity

Boditech AFIAS Infliximab Product Specifications

  • Medical-grade plastic and electronic components
  • Silent
  • New
  • Analyzer-dependent
  • Fluorescent ImmunoAssay (FIA)
  • According to kit insert & analyzer
  • Automatic/Manual (Instrument Required)
  • Analyzer-dependent
  • Quantitative determination of infliximab levels
  • Yes
  • IVD Diagnostic Cartridge
  • Single-use, quantitative, rapid, reliable, easy handling
  • White with printed labels
  • Dependent on analyzer
  • No
  • As per manufacturer: typically up to 12 months
  • Laboratory in-vitro diagnostics
  • Compatible Boditech AFIAS analyzer (external power required)
  • Single-use, lightweight cartridge
  • Store at 2-8C, protect from direct sunlight
  • IVD Cartridge for use with Boditech AFIAS system
  • Infliximab assessment in serum
  • Clinical accuracy and sensitivity validated
  • Cartridge size compatible with AFIAS system
  • Cartridge is portable; analyzer may not be
  • Digital, quantitative
  • Single-use
  • AFIAS Analyzer
  • Barcode on each cartridge
  • Therapeutic drug monitoring for patients treated with infliximab (Remicade®)
  • CE-IVD approved
  • Individually foil packed
  • Approximately 10-20 minutes per run
  • Test cartridge, buffer, desiccant pouch, instruction leaflet
  • Exclusive for Boditech AFIAS platforms
  • Analyzer auto-calibrated via cartridge barcode
  • Specified in kit insert
  • Fluorescent-labeled antibody for infliximab
  • Serum

Product Description

Brand                   Boditech

Sample Type       Serum/ Plasma/ WB

SMFP-74              24T

CAT No                SMFP-75

Biomarker           Therapeutic Drug Monitoring

Therapeutic Drug Monitoring (TDM) is to optimize biologic treatment for an individual patient. AFIAS Infliximab allows for reliable measurement of Infliximab drug levels using just a small amount of human serum, plasma, or whole blood, delivering results in 10 minutes. This allows clinicians to confirm the drug levels of Infliximab immediately before the next administration.



Precise Therapeutic Drug Monitoring

The AFIAS Infliximab test delivers clinically validated, quantitative measurement of infliximab levels in serum. This enables healthcare providers to effectively monitor therapy, ensure optimal dosing, and enhance patient outcomes. The assay is highly reliable due to its fluorescence-based detection and analyzer-driven calibration.


Rapid, Easy, and Reliable Operation

With a turnaround time of only 10-20 minutes, the AFIAS Infliximab cartridge lets laboratories act quickly. Designed for ease of handling, the single-use kit minimizes risks of cross-contamination and user error. Automated calibration ensures high consistency, while digital output makes interpretation straightforward.


Seamless AFIAS System Compatibility

Engineered for exclusive use with Boditech AFIAS analyzers, the cartridge integrates smoothly into your existing workflow. Each cartridge features barcode-based traceability and is stored at 2-8C for longevity. Compact and portable, the test supports flexible laboratory practice while upholding rigorous diagnostic standards.

FAQ's of Boditech AFIAS Infliximab:


Q: How does the Boditech AFIAS Infliximab test work?

A: The AFIAS Infliximab test employs a fluorescent-labeled antibody to quantitatively measure infliximab levels in serum. Once the sample is added to the cartridge and inserted into a compatible Boditech AFIAS Analyzer, the system automatically calibrates via cartridge barcode and provides digital results within 10-20 minutes.

Q: What are the main benefits of using the AFIAS Infliximab cartridge for drug monitoring?

A: This single-use, quantitative cartridge provides rapid, accurate results, supports precise therapeutic management, simplifies workflow with auto-calibration, and reduces cross-contamination risks. Its digital output ensures easy integration with laboratory processes and enhanced decision-making for infliximab therapy adjustments.

Q: When and where should the AFIAS Infliximab test be used?

A: The test is intended for laboratory use to monitor serum infliximab levels in patients undergoing Remicade therapy. It is suitable when timely dose adjustments are required for optimal therapeutic outcomes, and is designed exclusively for use in conjunction with the Boditech AFIAS Analyzer.

Q: What components are included in the AFIAS Infliximab kit?

A: Each kit contains a single-use test cartridge, buffer, desiccant pouch, and instruction leaflet. The cartridge is individually foil-packed and features a barcode for lot traceability. An AFIAS Analyzer instrument is required for processing the test.

Q: How should the AFIAS Infliximab test cartridge be stored and handled?

A: Store the cartridge at 2-8C and protect it from direct sunlight. Allow the cartridge to reach room temperature before use, and ensure it is not expired by checking the shelf life as indicated by the manufacturer.

Q: What is the detection principle and how is accuracy assured?

A: The test operates on the Fluorescent ImmunoAssay (FIA) principle, using fluorescent-labeled antibodies specific for infliximab. Accuracy and sensitivity are clinically validated, with automated instrument calibration ensuring consistent and reliable results.

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