Product Details:
Minimum Order Quantity | 5 Piece |
ICMR Approved | Yes |
Brand | Nu Life Care |
Model Name/ Number | Abchek Filariasis IgM/Igm |
Number of Reactions(Preps)/Kit | test kit |
Sample Type | Blood |
The Nu Life Care Abchek Filariasis IgM/IgG Combo Rapid Test is a lateral flow immunochromatographic assay used for the qualitative detection of IgM and IgG antibodies specific to filarial parasites in human blood, serum, or plasma. This test helps in diagnosing lymphatic filariasis, a parasitic disease transmitted through mosquito bites, commonly caused by Wuchereria bancrofti.
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Key Features
Dual Antibody Detection: Simultaneously detects IgM (recent infection) and IgG (past or ongoing infection)
Rapid Results: Provides results within 15–20 minutes
Easy to Use: Simple, user-friendly format for point-of-care testing
High Accuracy: Strong sensitivity and specificity for clinical reliability
Versatile Sample Use: Works with whole blood, serum, or plasma
No Equipment Needed: Ideal for remote areas or field diagnostics
Clear Visual Interpretation: Distinct test/control line visibility
Individually Packed: Hygienic, sealed single-use test kits
Industries Served
Hospitals & Clinics
Public Health and Epidemiology Programs
Diagnostic Laboratories
Rural Health Camps
Tropical Disease Research Centers
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Product Details:
Minimum Order Quantity | 5 Piece |
ICMR Approved | Yes |
Result Time (Rapid Kits) | 10-15 min |
Sample Type | Blood |
Sample Volume | 10 20 |
Product Type | Rapid |
The Nu Life Care Abchek Leptospira IgM/IgG Rapid Test is a qualitative, lateral flow immunoassay for the detection of IgM and IgG antibodies against Leptospira bacteria in human serum, plasma, or whole blood. It assists in the early diagnosis of leptospirosis, a bacterial infection often transmitted through contaminated water or animal urine, especially in tropical and subtropical regions.
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Dual Antibody Detection: Simultaneously identifies IgM (early stage) and IgG (later or past infection)
Rapid Results: Provides accurate results in 15–20 minutes
Multiple Sample Types: Accepts whole blood, serum, and plasma samples
No Equipment Needed: Ideal for point-of-care and field diagnostics
User-Friendly Design: Simple procedure suitable for professionals and trained healthcare workers
High Accuracy: Strong sensitivity and specificity
Compact and Sealed Packaging: Individually packed for single-use and safe handling
Hospitals and Diagnostic Laboratories
Infectious Disease Clinics
Public Health Programs
Rural and Remote Healthcare Facilities
Emergency and Disaster Relief Units
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
Sample Type | Blood |
Size | 96 tests per kit |
ICMR Approved | Yes |
Brand | Qiagen |
List no | R |
The NanoDrop One is an advanced microvolume UV-Vis spectrophotometer used to analyze DNA, RNA, and protein with as little as 1–2 µL of sample. It features patented sample-retention technology and Acclaro Sample Intelligence, enabling accurate contaminant detection and true concentration calculation. Ideal for rapid and reliable nucleic acid and protein quantification in research and diagnostics.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 98508 70860, +91 84461 74263.1–2 µL sample volume for fast, direct measurement
Full-spectrum UV-Vis analysis (190–850 nm)
Acclaro™ Sample Intelligence Technology: identifies contaminants and corrects readings
Built-in touchscreen with Android OS; standalone operation
Quantifies DNA, RNA, and proteins (A260, A280, A205, colorimetric assays)
Cuvette option available with NanoDrop OneC model for kinetics & dilute sample
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
Sample Type | Blood |
Size | 100 |
ICMR Approved | Yes |
Brand | Qiagen |
List no | R |
The artus VZV RG PCR Kit is a ready-to-use system designed for the detection and quantification of Varicella-Zoster Virus (VZV) DNA using real-time PCR. It is optimized for use with the Rotor-Gene Q MDx instrument and is intended for in vitro diagnostic use. The kit utilizes a specific amplification of an 82 bp region of the VZV genome, providing high sensitivity and specificity for VZV detection.
Note – The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 98508 70860, +91 84461 74263 Key FeaturesHigh Sensitivity
Dual Fluorescence Channels
Quantitative Analysis
Disclaimer - UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer
Product Details:
Sample Type | Blood |
Usage/Application | Hospital |
Size | 100 |
List no | R |
Brand | Qaigen |
The artus HBV QS-RGQ Kit is a ready-to-use, real-time PCR assay developed for the quantitative detection of hepatitis B virus (HBV) DNA. It is optimized for use with the QIAsymphony RGQ system, integrating automated sample preparation with the Rotor-Gene Q instrument for amplification and detection. The kit targets a conserved 134 bp region of the HBV genome and includes an internal control to monitor for PCR inhibition, ensuring reliable and accurate results. It is intended for in vitro diagnostic use.
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Key FeaturesComprehensive Genotype Coverage
Integrated Internal Control
Optimized for Automation
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
ICMR Approved | Yes |
Brand | Qaigen |
Usage/Application | laoratory |
Storage Temperature | -20 DegreeC |
Test Time | 2 hr |
List no | R |
The Qiagen artus BK Virus RG PCR Kit is a ready-to-use, in vitro diagnostic assay designed for the qualitative detection of BK virus (BKV) DNA using real-time PCR technology. It is optimized for use with the Rotor-Gene Q instruments, providing reliable and sensitive detection of BKV in clinical samples. This assay is particularly useful in monitoring BKV infections in immunocompromised patients, such as kidney transplant recipients.
Note – The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 98508 70860, +91 84461 74263Key FeaturesSpecific Detection
Internal Control
Quantitation Standards
Disclaimer - UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer
Product Details:
ICMR Approved | Yes |
Number of Reactions(Preps)/Kit | 50 |
Result Time (Rapid Kits) | 2-3 hr |
Sample Type | Blood |
Product Type | Viral DNA Detection Kit |
List no | R |
Brand | Qaigen |
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Key Features:
Real-time fluorescence detection
High throughput capability
Rapid thermal cycling
Touchscreen interface
Compatibility with multiple assay formats
Product Details:
ICMR Approved | No |
Number of Reactions(Preps)/Kit | 50 |
Result Time (Rapid Kits) | 2 to 3 hours |
Packaging Type | reagent kit packaging |
Brand | Qaigen |
List no | R |
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Key Features:High Sensitivity: The Artus Parvo B19 LC PCR Kit has an analytical sensitivity of 125 IU/ml, ensuring reliable detection even at low viral loads.
Internal Control: Each kit includes a heterologous amplification system to detect possible PCR inhibition, ensuring accurate results.
Quantification Standards: External positive controls (Parvo B19 LC QS 1–5) are provided, allowing for the determination of pathogen load.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
Minimum Order Quantity | 5 Kit |
ICMR Approved | Yes |
Number of Reactions(Preps)/Kit | 50 Kits |
Result Time (Rapid Kits) | 15-20 minutes |
Sample Type | Blood |
In Deal | Kit |
Brand | Nu Life Care |
The Nu Life Care Abchek HIV 1 & 2 Rapid Test is a lateral flow immunochromatographic assay designed for the qualitative detection of antibodies to HIV-1 and HIV-2 in human serum, plasma, or whole blood. It is used as a screening tool for HIV infection, providing fast and reliable results in clinical, field, and point-of-care settings.
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Key FeaturesDual HIV Detection: Identifies antibodies to both HIV-1 and HIV-2
Rapid Results: Delivers accurate results within 15–20 minutes
Sample Flexibility: Accepts whole blood, serum, and plasma
High Sensitivity and Specificity: Clinically reliable for early screening
Simple Procedure: Requires no special equipment or laboratory setup
Ideal for Field Use: Compact and individually packaged for point-of-care deployment
Clear Visual Indicators: Easy-to-read control and test lines for accurate interpretation
Hospitals and Clinics
Blood Banks and Donor Screening Centers
Public Health Programs
Community Health Camps
Diagnostic Laboratories
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
Minimum Order Quantity | 5 Kit |
ICMR Approved | Yes |
Sample Type | Blood |
Number of Test/Kit | 50 |
Brand | Nu Life Care |
Result Time | 15-20 min |
Shelf Life | 24 Months |
Product Type | Hepatitis C Virus (Hcv) |
The Nu Life Care Abchek HCV Rapid Test is a lateral flow immunoassay intended for the qualitative detection of antibodies to the Hepatitis C Virus (HCV) in human serum, plasma, or whole blood. This test is used as a screening tool for HCV infection, offering a quick and reliable means of identifying individuals exposed to the virus.
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Fast Results: Delivers results within 15–20 minutes
Multiple Sample Types: Compatible with whole blood, serum, or plasma
High Accuracy: Designed with high sensitivity and specificity for clinical reliability
Easy to Use: Simple test procedure for both laboratory and point-of-care use
No Equipment Required: Ideal for remote or low-resource settings
Clear Visual Interpretation: Easily distinguishable control and test lines
Sterile and Compact Packaging: Individually packed for safe and hygienic use
Hospitals & Clinics
Diagnostic Laboratories
Public Health and Infectious Disease Programs
Community Screening Campaigns
Blood Banks and Donation Centers
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
Minimum Order Quantity | 5 Kit |
ICMR Approved | Yes |
Sterile/ Non Sterile | Sterile |
Number of Reactions(Preps)/Kit | 50 Kit |
Brand | Nu Life Care |
Packaging Type | Box |
Usage/Application | Clinic |
Sample Type | Blood |
Disposable/ Reusable | Disposable |
Model Name/ Number | Abcheck Dengue Combo (NS1 and Igm/Igm) |
The Nu Life Care Abchek Dengue Combo Rapid Test is a lateral flow immunoassay designed for the simultaneous detection of Dengue NS1 antigen, IgM, and IgG antibodies in human serum, plasma, or whole blood. This combo test enables early diagnosis (via NS1) and differentiation between recent (IgM) and past (IgG) infections, providing a comprehensive diagnostic solution for dengue fever.
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Key Features
3-in-1 Detection: Identifies NS1 antigen, IgM, and IgG antibodies
Rapid Turnaround: Delivers results within 15–20 minutes
Comprehensive Diagnosis: Effective in both acute and later stages of infection
Multiple Sample Types: Suitable for serum, plasma, and whole blood
No Lab Equipment Needed: Ideal for point-of-care and field use
Simple to Use: Easy procedure with clear visual interpretation
Hygienic and Safe: Individually packed, single-use kits
Hospitals and Emergency Departments
Clinical and Diagnostic Labs
Public Health Units
Mobile Testing Camps
Tropical Disease Surveillance Programs
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
Usage/Application | Laboratory |
Size | 50 |
ICMR Approved | No |
List no | R |
Brand | Qaigen |
The artus M. tuberculosis RG PCR Kit is a real-time PCR assay designed for the detection of DNA from all members of the Mycobacterium tuberculosis complex (MTBC), including M. tuberculosis, M. africanum, M. bovis, M. bovis BCG, M. microti, and M. pinnipedii. Utilizing ready-to-use reagents and optimized protocols, this kit facilitates rapid and reliable detection of MTBC DNA in various sample types. It is intended for research use only and is not for use in diagnostic procedures.
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Key FeaturesComprehensive Detection
Ready-to-Use Reagents
Internal Control
Quantitative Standards
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
ICMR Approved | Yes |
Test Duration | 2-4 hours |
Number of Reactions(Preps)/Kit | 24 reactions (preparations) per kit. |
Storage Temperature | -20 DegreeC to maintain reagent stability and performance. |
Test Time | 2-3 hrs |
Shelf Life | 12 months |
list no | R |
brand | Qaigen |
storage condition | -20 DegreeC |
no of test per kit | 25 |
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 98508 70860, +91 84461 74263.
Key Features:Target Mutations: Detects MPL W515L and MPL W515K mutations independently.
Technology: Utilizes real-time PCR on the Rotor-Gene Q and other compatible instruments.
Sensitivity: Optimized to detect mutations with a detection limit corresponding to 1.5% mutant allele frequency.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
Number of preps | 50 |
Brand | Qiagen |
Storage Temperature | -20 DegreeC |
Sample Amount | 10-20 |
list no | R |
The QIAGEN RNeasy FFPE Kit is designed for the purification of total RNA from formalin-fixed, paraffin-embedded (FFPE) tissue sections. Utilizing a specialized lysis and incubation protocol, the kit effectively reverses formaldehyde-induced crosslinking, ensuring the isolation of high-quality RNA suitable for downstream applications such as RT-PCR and qPCR.
Note – The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 98508 70860, +91 84461 74263Efficient Crosslink Reversal
High-Quality RNA Yield
Integrated DNase Treatment
Disclaimer - UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer
Product Details:
Number of Reactions(Preps)/Kit | 25 Kits |
ICMR Approved | Yes |
Result Time (Rapid Kits) | 20 minutes |
Sensitivity | 100% |
Brand | Meril |
List No. | R |
Model No. | RPDHIV-03 |
Antigen/Antibody Detection | - HIV-1: gp41, gp120 - HIV-2: gp36 - p24 antigen (HIV core protein) |
Sample Types | Human serum, plasma, whole blood |
Assay Buffer | 3 drops |
Assay Buffer Volume | 3 drops |
Test Type | One-step immunochromatographic assay |
Test Window Period | Reduced due to early p24 antigen detection |
Key Features:
Sensitivity: 100%
Specificity: 100%
Analytical Sensitivity of HIV p24 Ag: 100 IU/ml using NIBSC Standard, U.K. Code No. 90/636
Detection Markers:
HIV p24 Antigen
HIV-1 (gp41, gp120) and HIV-2 (gp36) antibodie
Detects Antibodies: IgG, IgM, IgA