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Standard F Legionella Ag FIA

Standard F Legionella Ag FIA

Product Details:

  • Display Type Requires Reader (Not Included)
  • Frequency Single Use
  • Shelf Life 12 Months
  • Instruments Type Rapid Test Kit
  • Measurement Range Qualitative
  • Accuracy >95%
  • Function Detects Legionella pneumophila antigen
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Standard F Legionella Ag FIA Price And Quantity

  • 1000 Box

Standard F Legionella Ag FIA Product Specifications

  • Silent Operation
  • Requires Reader (Not Included)
  • Single Use
  • White
  • New
  • Plastic, Diagnostic Reagents
  • No
  • 100-240 V AC
  • Store at 2-8C
  • Yes
  • Yes
  • Fluorescent Immunoassay (FIA)
  • >95%
  • Detects Legionella pneumophila antigen
  • Rapid Detection, Easy to Use, Reliable Results, High Sensitivity & Specificity
  • Diagnostic
  • External Power Supply
  • Hospital
  • Lightweight
  • Manual/Automatic
  • Standard Packing, Compact Size
  • Qualitative
  • 12 Months
  • Low Power Consumption
  • Rapid Test Kit
  • 15-20 Minutes
  • Fluorescent Immunoassay Analyzer Kit
  • Immunochromatography
  • Legionella pneumophila serogroup 1 antigen detection in urine
  • Urine
  • 25 Tests / Kit

Product Description



Discover the Reserve Standard F Legionella Ag FIA, an elite rapid detection kit for Legionella pneumophila serogroup 1 antigens in urine. This preeminent solution employs unmatchable fluorescent immunochromatography technology, delivering results within 15-20 minutes. Featuring a reduced price, this diagnostic kit encompasses 25 tests per pack, ideal for hospitals and laboratories requiring reliable, high-sensitivity testing. Its compact, lightweight design ensures portability, while silent operation and low power consumption guarantee effortless integration. Experience remarkable accuracy over 95%, picturesque simplicity, and real-time, manual or automatic functionality.

Versatility in Medical Diagnostics

The Standard F Legionella Ag FIA is extensively used by hospital professionals, laboratory technicians, and diagnostic practitioners. Suitable for use in medical centers, clinics, and healthcare institutions, this unmatchable rapid test kit excels in the detection of Legionella pneumophila antigens. Its application places range from emergency departments to infectious disease labs, providing exceptional support in both routine screening and outbreak management with preeminent accuracy and dependable results.


Packaging, Export, and Delivery Process

Standard F Legionella Ag FIA is securely packaged in standard packing, preserving quality throughout transport services. Each quotation includes comprehensive export details for international markets, especially those in India and neighboring countries. Main export markets feature hospitals, clinics, and distributors globally. Upon order confirmation, the product is swiftly handed over for prompt delivery, ensuring a seamless supply chain with minimal lead time and dependable shipment tracking for all wholesale or retail requirements.


FAQ's of Standard F Legionella Ag FIA:


Q: How does the Standard F Legionella Ag FIA detect Legionella pneumophila antigen?

A: The kit uses immunochromatography and advanced fluorescent immunoassay technology to qualitatively detect Legionella pneumophila serogroup 1 antigen in urine, providing rapid and accurate results.

Q: What makes this Legionella Ag FIA kit preeminent compared to others?

A: Its unmatchable accuracy of over 95%, rapid assay time of 15-20 minutes, elite sensitivity and specificity, and portable design make it a standout choice for fast, reliable diagnostics.

Q: Where can the Standard F Legionella Ag FIA be used safely?

A: This kit is designed for use in hospitals, clinics, laboratories, and other healthcare institutions, enabling effective and safe testing in various medical environments.

Q: When should this rapid test be used during patient evaluation?

A: The test is ideal for early diagnosis and screening in suspected Legionella pneumophila infection cases, particularly during outbreaks or when rapid intervention is critical.

Q: What is the process for using the kit?

A: Simply collect a urine sample, follow the provided instructions for manual or automatic analysis using a compatible reader, and obtain qualitative results in real time within 15-20 minutes.

Q: What storage requirements must be followed for this diagnostic test kit?

A: To maintain optimal performance, store the kit at temperatures between 2-8C and ensure it is used within its 12-month shelf life.

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