Boditech AFIAS Anti-Mullerian Hormone (AMH)

Boditech AFIAS Anti-Mullerian Hormone (AMH)

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Product Details:

Display Type Not Applicable for Cartridge (Result displayed on analyzer)
Features Fast result, high sensitivity, integrated sample processing, ready-to-use single-use cartridge
Frequency Not Applicable for Cartridge
Shelf Life 12 months from manufacturing date
Accuracy 95% (as per manufacturers validation)
Function Quantitative measurement of AMH as an ovarian reserve marker
Instruments Type Diagnostic Reagent Cartridge
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Boditech AFIAS Anti-Mullerian Hormone (AMH) Price And Quantity

Boditech AFIAS Anti-Mullerian Hormone (AMH) Product Specifications

Accuracy 95% (as per manufacturers validation)
Voltage Not Applicable for Cartridge
Power Consumption Not Applicable for Cartridge
Material Plastic Cartridge with Integrated Test Strip and Reagents
Measurement Range 0.0820.0 ng/mL
Operating Type Automated
Power Source Not required for Cartridge (Analyzer operated by external power)
Frequency Not Applicable for Cartridge
Features Fast result, high sensitivity, integrated sample processing, ready-to-use single-use cartridge
Weight Approx. 15 g per cartridge
Color White Cartridge
Dimension (L*W*H) Cartridge: 120 x 25 x 10 mm (approx)
Shelf Life 12 months from manufacturing date
Real-Time Operation Yes
Storage Instructions Store at 2-8C, away from direct sunlight
Portable Yes (used with compatible AFIAS analyzer)
Condition New
Use Used for quantitative determination of Anti-Mullerian Hormone (AMH) in human serum, plasma, or whole blood
Wall Mounted No
Usage Type In-vitro Diagnostic
Noise Level Silent Operation
Technology Fluorescence Immunoassay (FIA)
Display Type Not Applicable for Cartridge (Result displayed on analyzer)
Equipment Type Immunoassay Analyzer Reagent Cartridge
Instruments Type Diagnostic Reagent Cartridge
Function Quantitative measurement of AMH as an ovarian reserve marker

Calibration Factory calibrated; no user calibration required
Compatible Analyzer AFIAS-6 and AFIAS-1 analyzers
Regulatory Status IVD CE marked
Disposal Biohazard; dispose according to local regulations
Time to Result Approximately 814 minutes per test
Sample Type Serum, Plasma, or Whole Blood
Test Principle Sandwich Immunoassay using fluorescent-labeled antibody
Sensitivity 0.08 ng/mL (Limit of Detection)
Lot Traceability Barcoded for automatic recognition in analyzer
Kit Components Integrated cartridge, buffer solution (if applicable), instruction sheet
Test Throughput Single test per cartridge
Intended User For professional use only

Product Description

Brand Boditech

Sample Type Serum/ Plasma/ WB

Pack Size 24T

CAT No SMFP-62

Biomarker Hormone Function

AMH levels help predict the remaining egg reserve. This can tell a lot about the reproductive issues, including the onset of menopause, amenorrhea, polycystic ovary syndrome. This test also tells the expected response to controlled ovarian hyperstimulation to achieve pregnancy in IVF.

Rapid, Accurate Ovarian Reserve Testing

Designed for professional use, the AFIAS AMH cartridge empowers healthcare providers with fast and reliable ovarian reserve assessment, optimizing fertility evaluation and reproductive planning. Its high sensitivity (0.08 ng/mL) and rapid turnaround time allow clinics to deliver timely results to patients while maintaining workflow efficiency.

One-Step, Automated Testing Workflow

The cartridge is ready-to-use with an integrated test strip and reagents, streamlining the diagnostic process. Simply add the required sample type (serum, plasma, or whole blood) to the cartridge and insert it into the compatible AFIAS analyzer. The test is fully automated-no manual calibration is needed-and the analyzer displays results in real time.

Innovative Design and Compliance

Each cartridge features barcoded lot traceability for seamless identification and traceability within the laboratory setting. The product is CE marked for IVD use in India and comes with 12 months' shelf life when stored at 2-8C. Designed for safety and simplicity, the cartridge and materials are for single-use and must be disposed of as biohazard waste according to local regulations.

FAQ's of Boditech AFIAS Anti-Mullerian Hormone (AMH):

Q: How is the Boditech AFIAS AMH cartridge used in clinical settings?

A: To use the Boditech AFIAS AMH cartridge, a professional adds a patient's serum, plasma, or whole blood sample into the cartridge and inserts it into either the AFIAS-1 or AFIAS-6 analyzer. The system processes the sample using an automated fluorescence immunoassay and displays the AMH level within 8-14 minutes.

Q: What are the main benefits of using this AMH test cartridge for ovarian reserve assessment?

A: Key benefits include rapid results (8-14 minutes), high sensitivity (0.08 ng/mL), quantitative accuracy (95%), minimal sample handling, and complete automation without user calibration. This allows for timely and reliable ovarian reserve evaluation crucial for fertility assessment and reproductive health decisions.

Q: When should the AFIAS AMH test be performed?

A: The AFIAS AMH test is typically performed when healthcare providers need to evaluate a woman's ovarian reserve-commonly in fertility workups, before certain gynecological treatments, or when investigating reproductive disorders. The test can be ordered whenever accurate AMH measurement is clinically indicated.

Q: Where can this cartridge be used and who should use it?

A: This cartridge is intended for use in clinical laboratories, fertility clinics, and hospital diagnostic centers. It is strictly for use by professional healthcare personnel trained in in-vitro diagnostic testing, compatible only with AFIAS-1 and AFIAS-6 analyzers.

Q: What types of samples are compatible with the AFIAS AMH cartridge?

A: The cartridge is validated for serum, plasma, or whole blood samples, providing flexibility for diverse patient needs and streamlined blood collection practices in the clinical environment.

Q: How should the AFIAS AMH cartridges be stored and disposed of?

A: Cartridges should be stored at 2-8C, away from direct sunlight to ensure reagent integrity up to their 12-month shelf life. After use, each cartridge must be disposed of as biohazard waste according to local regulatory requirements.

Q: What is the process of result interpretation with the analyzer used for this cartridge?

A: Once the cartridge is processed in the AFIAS analyzer, the device automatically detects, measures, and reports the AMH concentration in ng/mL. The lot barcode on each cartridge ensures precise traceability, and the digital display on the analyzer enables immediate review and electronic documentation of results.

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