Maleria PF -PV AG SD-BIO

Name: Maleria PF -PV AG SD-BIO
Brand: Infinity Diagnochem

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MOQ : 10 Pieces

Maleria PF -PV AG SD-BIO Specification

Purity
>99%

Storage Instructions
Store at 2-30C, keep away from sunlight, do not freeze

Ph Level
Neutral

Shelf Life
24 months from manufacturing date

Physical State
Solid (Cassette/device format)

Packaging Type
Individually foil packed device with desiccant, box packing

Size
Standard size cassette

Usage
For in vitro diagnostic use, suitable for clinical and laboratory settings

Grade
Diagnostic

Type
Malaria Rapid Test Device

Application
Qualitative detection of Plasmodium falciparum (PF) and Plasmodium vivax (PV) antigens in human whole blood

Appearance
Solid Strip Device

Purity(%)
>99%

Minimum Sample Volume
5 µL

Result Time
10-20 minutes

Test Principle
Immunochromatographic assay

Manufactured By
SD Bioline

Specificity
>99%

Lot Number
Printed on packaging

Sensitivity
>99% for PF and PV antigen detection

Control Line
Built-in for procedural validity

Disposal
Biohazard, follow laboratory waste guidelines

Sample Type
Whole blood (capillary or venous)

Reading Window
Dual window for PF and PV results

Maleria PF -PV AG SD-BIO Trade Information

Minimum Order Quantity
10 Pieces

Supply Ability
100 Pieces Per Month

Delivery Time
7 Days

About Maleria PF -PV AG SD-BIO

Discover the Maleria PF -PV AG SD-BIO, a cost-effective rapid test device that delivers monumental accuracy for malaria detection. With over 99% sensitivity and specificity, this cutting-edge device identifies Plasmodium falciparum and Plasmodium vivax antigens within an imposing 10-20 minute result window. Boasting a solid cassette format and dual reading windows, it's engineered by SD Bioline for reliability in clinical and laboratory settings. Take advantage of this soaring diagnostic advancement-a limited time offer for discerning professionals across India seeking uncompromised quality in malaria testing.

Versatile and Trusted in Diagnostics

Maleria PF -PV AG SD-BIO is a diagnostic-grade rapid test device designed for qualitative detection of PF and PV antigens directly from human whole blood. Ideal for use in hospitals, clinics, and laboratory environments, it features a dual reading window for separate PF and PV results. With its minimal sample requirement and built-in control line, the device is both user-friendly and highly dependable for routine and emergency malaria screening.

Strong Supply Ability and Efficient Delivery

Our supply chain for Maleria PF -PV AG SD-BIO guarantees a steady and reliable provision to meet soaring demands in India and export markets. Delivery timelines begin promptly upon receipt of a purchase order and finalized quotation, ensuring your stock remains unhindered. Trusted dealers and wholesalers can count on swift turnaround times and robust packaging, making procurement straightforward for healthcare facilities and professionals nationwide and abroad.

FAQ's of Maleria PF -PV AG SD-BIO:

Q: How does the Maleria PF -PV AG SD-BIO test for malaria antigens?

A: The Maleria PF -PV AG SD-BIO uses an immunochromatographic assay to detect Plasmodium falciparum and Plasmodium vivax antigens qualitatively from whole blood samples, delivering reliable results in just 10-20 minutes.

Q: What sample type and volume are needed for performing this test?

A: This device requires only 5 L of whole blood, which can be collected from either capillary or venous sources, making the process quick and convenient.

Q: Where can this rapid test be effectively utilized?

A: Maleria PF -PV AG SD-BIO is suitable for use in clinical laboratories, hospitals, and diagnostic centers, supporting healthcare professionals in both routine screenings and outbreak responses.

Q: When will I receive my product after placing an order?

A: Once your purchase order and quotation are confirmed, delivery commences promptly, with timelines varying based on location and shipment method. Our efficient logistics ensure timely arrival.

Q: What benefits does this test offer over traditional malaria testing methods?

A: With over 99% sensitivity and specificity, the device ensures swift and accurate diagnosis, requires minimal sample volume, and provides a dual reading window, streamlining workflow and patient management.

Q: How should I dispose of the test device after use?

A: Because it is classified as biohazardous waste, follow established laboratory waste disposal protocols to ensure safe handling and environmental compliance.

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