INTENDED USE The HIV TRI-DOT test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 & HIV-2 antibodies (IgG) in human serum or plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane. The test is a screening test for Anti HIV-1 and HIV-2 and is for in vitro diagnostic use only.
Rapid visual test ,based on Flow Through Technology.
Differential detection of HIV-1 & HIV-2.
Detection of group O & subtype C.
Use of envelop antigens gp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2.
100% sensitivity & 100% specificity as per WHO Evaluation.
Shelf life 15 months at 2-8°C
Available in convenient pack sizes-10 Tests, 50 Tests and 100 Tests.
INTENDED USE The 4th Generation HCV TRI-DOT is a rapid, visual, sensitive and qualitative in vitro diagnostic test for the detection of antibodies to Hepatitis C virus in human serum or plasma. It has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigen.
Based on “Flow Through Technology”, which is similar to Elisa technology because of involvement of washing steps at various levels to enhance the specificity.
Use of highly purified HCV antigens for Core, NS3, NS4, NS5 immobilized on the device.
Detection of all the subtypes of HCV.
Results within 3 minutes.
In built quality control dot which validates the test.
100% Sensitivity & 98.9% Specificity as per WHO evaluation.
HEPACARD is visual, rapid, sensitive and accurate one step immunoassay for the qualitative detection of Hepatitis B surface antigen (HBsAg) in Human serum or plasma.The assay is intended to be used as an aid in the recognition and diagnosis of acute infections and chronic infectious carriers of the Hepatitis B Virus(HBV).
Detects all the 11 subtype of HBsAg.
Antigen Sensitivity- 0.5 ng/ml.
No sample preparation required.
See through Device for easy result interpretation.
Shelf life-24 months at 2-30°C.
100% Sensitivity & 98.0% Specificity by WHO Evaluation.
ADVANTAGE MALARIA PAN +Pf CARD is a rapid, visual and sensitive immunoassay for the qualitative diagnosis of infection with P.falciparum and other Plasmodium species (P.falciparum/P.vivax/P.malariae/P.ovale) in human whole blood only.
Detects P.f. (HRP-2) and PAN(pLDH)
Individually pouched Single tests- Practical & Safe
ADVANTAGE P.f MALARIA CARD is a rapid, visual and sensitive immunoassay for the qualitative diagnosis of P.falciparum(P.f) specific Histidine-rich protein-(P.f. HRP-2) in human whole blood only.
SALIENT FEATURES Rapid visual antigen based test for detecting infection with P.falciparum (HRP-2) malaria parasite in whole blood. Excellent Sensitivity & Specificity as per WHO Malaria RDTs Evaluation. Sensitivity of 50 -100 parasites per µl of blood. See through Device for easy result interpretation. Longer shelf life -24 months, storage at 4-30° C. Results within 20 minutes
DENGUE TEST / DENGUE RAPID TEST (Dengue NS1 Ag + IgM/IgG Antibodies)
INTENDED USE Dengue Day 1 Test is a rapid solid phase immuno-chromatographic test for the qualitative detection of Dengue NS1 Antigen and differential detection of IgM and IgG antibodies to Dengue virus in Human serum/plasma. This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of Dengue infection & presumptive diagnosis between primary and secondary Dengue infection.
First line testing kit for detecting dengue infection from day 1 using NS1 Antigen & differential detection of IgM & IgG Antibodies.
Diagnosis of both Primary & Secondary Infection.
Detects all 4 serotypes of Dengue virus
Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4).
DENGUE TEST / DENGUE RAPID TEST / DENGUE NS1 Ag RAPID TEST
Advantage Dengue NS1 Ag card is a rapid solid phase Immuno-chromatographic test for the qualitative detection of Dengue NS1 Antigen in Human serum /Plasma.This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of Dengue Infection.
Rapid test based on lateral flow technique.
Detection of Dengue in the seronegative stage i.e. from Day 1 of fever.
Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4).
Advantage Typhi IgM & IgG Card is a rapid solid phase immuno-chromatographic test for the qualitative differential and simultaneous detection of salmonella typhi (S. typhi) IgM and IgG antibodies in human serum / plasma. This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of typhoid infection and in the determination of recent and past infection.
SALIENT FEATURES Rapid qualitative test for differential detection of Salmonella typhi (S.typhi) IgM and IgG Antibodies in Human Serum / Plasma Determination of both recent and past infection Results within 20 minutes Bio-hazard free, fully covered, see-through Device Simple & Easy to use Test Procedure No Instruments required Long Shelf Life: 18 months at 2-30ºC Convenient Packsize: 50 Tests
Dengue NS1 Antigen FP is a rapid solid phase immuno- chromatographic test for the qualitative detection of Dengue NS1 Antigen in human Whole Blood/ Serum/ Plasma. This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of dengue infection.
Rapid ,visual test for the qualitative detection of Dengue NS1 Antigen in whole blood/serum/Plasma.
Sample can be taken from Finger prick and sample required is 4µl.
Based on Sandwich principle.
Detection of Dengue in Seronegative stage i.e From Day 1 of fever.
Detection of all 4 serotypes of dengue virus.
Reliable diagnosis of both primary and secondary infection.
100% Sensitivity & 99.96 % Specificity.
Shelf life: 24 month at 2-30 °C
Convenient pack Size: 10 Test & 50 Test.
Evaluated By Referral Medical college / Hospitals /Research institutes / Labs.
MICROLISA HIV is an in-vitro qualitative enzyme immunoassay for the detection of antibodies to HIV-1 and /or HIV-2 in human serum or plasma. It is intended for screening of blood donors or other individuals at risk for HIV-1 and HIV-2 infection and for clinical diagnostic testing.
Use of Envelope Antigens gp41,C terminus of gp120 for HIV-1& gp36 for HIV-2.
Detection of Group O & subtype C for HIV-1 prevalent in India.
The 3rd generation HCV Microlisa is an in vitro qualitative enzyme linked immunosorbent assay for the detection of antibodies against HCV (anti-HCVs) in human serum or plasma. The kit is basically intended to screen blood donations to identify and eliminate the infected units of blood and for clinical diagnostic testing.
3rd Generation Assay
Unique combination of HCV antigens for E1, E2, Core, NS3, NS4 & NS5
Break-away microwell strips
Based on Indirect Elisa principle
Colour coded reagents to monitor procedural steps.
HEPALISA is designed for in - vitro qualitative detection of Hepatitis B Surface antigen (HBsAg) in human serum or plasma and is used as a screening test for testing of collected blood prior to transfusion.
DENGUE NS1 Ag MICROLISA is designed for in vitro qualitative detection of Dengue NS1 antigen in human serum or plasma and is used as a screening test for testing of collected blood samples suspected for DENGUE. The kit detects all four subtypes; DEN1, DEN2, DEN3 & DEN4 of Dengue Virus.
First line testing kit for detecting infection with Dengue NS1 Ag.
Based on Direct Sandwich Elisa principle
Detection of all 4 serotypes of Dengue (DEN 1 – DEN 4)
We are India's highly reputed manufacturer of Blood Bags. The Company provides most advanced and sophisticated auto lines with High Standard and Solid Performance.
The manufacturing facility follows an integrated production system from raw materials to finished products,ensuring strict adherence to current Good Manufacturing Practice (cGMP).
NEW STANDARD FEATURES
Sticker Free Labels and Guaranteed Non-peelable plus now include information on most infectious disease.
A highly donor comfort redefined needle.
Tamper evident outlet ports.
Ribbed Safety Hub: Ribbed hubs provide excellent Traction control at time of insertion. Practically designed keeping in view for catering to busy centers.
Winged Needle Cover:Tamper evident and easy to remove, enhancing confidence and efficiency while maintaining needle high performance.
OPTIONAL VALUE ADDITION
Pre Donation Sampling Bag: Initial quantity of blood collected tends to contain contaminants from environment, bacteria etc from site of vein puncuture, which is diverted into the pre-donation sampling bag. Remaining blood being free from most such initial impurity, is collected in the Primary Bag.
Needle Safety Shield: Now Reduces the risk of needle stick injury by providing immediate shielding of needle after withdrawal.
Dialysis: It is an artificial way of cleaning & filtering of the blood and removal of excess fluid. Though it does not perform the full functions of the kidneys but those patients who takes recommended dialysis regularly remains relatively healthy and leads a near normal life.
There are two types of Dialysis - HD & PD
1. HD (HemoDialysis)
HD is conducted at hospital. In this therapy the blood is taken out of the body and is passed thru a machine for removal of waste and excess fluid. Cleaned blood goes back to the body. Normally this process takes about four hours and a patient has to undergo three such sessions in a week.
2. PD (Peritoneal Dialysis)-Home DialysisPD is conducted at home by the patient or his/her family members , in this therapy blood is cleaned within the body . Every person has peritoneal cavity,the membrane of peritoneum cavity helps in cleaning the blood and removal of excess water from the blood.
PD therapy does not require any equipments at home , in this process peritoneal dialysis fluid is infused into the peritoneum cavity. This fluid is kept in the peritoneum for 4 to 6 hours during this time waste product and excess fluid from the blood passes through the peritoneal and mixes with the fluid . This fluid is then removed from the body and fresh fluid is infused. The process of removal of affluent fluid (PD fluid mixed with waste products and excess fluid) and infuse of fresh PD fluid is called one exchange. Such four exchanges have to be performed everyday. Each exchange takes 25 to 30 minutes only. The patient is free to resume his normal life during the day except when doing exchange.
Chikungunya IgM Microlisa is designed for in vitro qualitative detection of Chikungunya IgM in human serum or plasma and is used as a screening test for testing of collected blood samples suspected for Chikungunya.
Principle : "MAC Capture ELISA".
Microwells Elisa test for detection of Chikungunya specific IgM Antibodies in Human serum & plasma.