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We offer a complete product range of Trustline HEV IgM Rapid Test, Trustline HAV IgM Rapid Test, Trustline Leptospira IgG/IgM Combo Rapid Test, trustline Filariasis IgG/IgM Rapid Test and Avecon MAXLINE DENGUE COMBO
A lateral flow chromatographic immunoassay for the qualitative detection of IgM antibodies to hepatitis E virus (HEV) in human serum or plasma.
Instant screening test
Detects IgM anti-HEV in serum or plasma
Evaluated with BBI HEV serum conversion and HEV mixed titer performance panels
Useful for identifying acute HEV infections
Each Kit Contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
10 L Capillary tubes
Sample Diluent (REF SB-R0095, 5mL/bottle)
One package insert (instruction for use)
The OnSite HAV IgM Rapid Test is a lateral flow immunoassay for the qualitative detection of IgM antibodies to hepatitis A virus (HAV) in human serum, plasma or whole blood.
Instant screening test
Detects IgM anti-HAV in serum, plasma and whole blood
Evaluated with BBI seroconversion panel (PHT903)
Useful for identifying acute HAV infections
The OnSite Leptospira IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay that can be performed within 15-20 minutes by minimally skilled personnel, and without the use of laboratory equipment.
Accuracy: 100% specificity and 100% sensitivity in comparison with a reference rapid test on the market
Cross Reactivity: No false positive results were observed on specimens from TP, HIV, Dengue, TB, Typhoid Ab , HBsAg, HCV Ab, HEV Ab, H.P Ab, HAV, HCG, RF, ANA, HAMA
Interference: No interference were seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 3.8 %; Heparin: 3, 000 U/L; Creatinine: 442 mol/L; Bilirubin: 20 mg/dL; EDTA: 3.4 mol/L; Hemoglobin: 2 g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L
Shelf life: 24 month
The TRUSTline Filariasis IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-lymphatic filarial parasites (W. Bancrofti and B. Malayi)in human serum, plasma or whole blood.
Use of conserved antigens allows pan-filaria tests to be applicable
Simple procedure provides alternative to diagnosis by blood smear
Use serum, plasma or whole blood
No restrictions on time of day for sample collection
| Method | Lateral flow Immunochromatographic Assay |
| Detection | Qualitative detection of dengue NS-1 Antigen |
| Specimen | Serum/Plasma |
Additional Information:
Delivery Time : 7 DAYS
Syphilis Ab Rapid Test (Strip) is an effective tool for blood bank screening and early detection of syphilis to facilitate treatment.
A lateral flow chromatographic immunoassay for the qualitative detection of antibodies including IgG, IgM, and IgA to Treponema pallidum (Tp) in human serum or plasma.
Detects IgG, IgM and IgA antibodies facilitating accurate screening during all stages of disease
Simple test procedure
Efficient, easy to interpret result
No additional equipment required
Room temperature storage
The TRUSTline Syphilis Ab Rapid Test is an effective tool for blood bank screening and early detection of syphilis to facilitate treatment.
A lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM, and IgA) to Treponema pallidum (Tp) in human serum or plasma.
Detects IgG, IgM, and IgA antibodies facilitating accurate screening during all stages of disease
Simple test procedure
Efficient, easy-to-interpret result
No additional equipment required
Room temperature storage
The TRUSTline Dengue Ag (NS1) Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of dengue NS1 antigen (DEN1, 2, 3, 4) in human serum, plasma or whole blood.
Product Features:
In-house developed fourth-generation rapid test aids in the diagnosis of an early acute infection, including primary or secondary infection
Detects NS1 antigen from all four dengue serotypes (DEN1, 2, 3, 4) in human serum, plasma or whole blood specimen
Simple assay procedure yields results within 20-25 minutes
Clinical Performance:
Limit of Detection: detection of NS1 protein in all 4 types of dengue virus lysate I, II, III, and IV. The limit of detection is 0.25 ng/mL as determined on recombinant dengue NS1 antigen from serotype 2 (DEN2)
Sensitivity: 100%
Specificity: 98.75% comparing to a commercial ELISA
Cross-Reactivity: no cross-reactivity found on 6-10 positive specimens from the 21 disease states, such as chikungunya, ZIKV, malaria, leishmania, Typhoid and others
No interference with some common substances, such as Albumin (60 g/L), Bilirubin (20 mg/dL), EDTA (3.4 mol/L), Glucose (55 mmol/L), Heparin (3, 000 U/L), Salicylic acid (4.34 mmol/L), Sodium citrate (3.8%), Human IgG (1, 000 mg/dL)
TheOnSiteH. pylori Ag Rapid Test is a lateral flow chromatographic immunoassay for qualitative detection ofH. pyloriantigen in human fecal specimen. It is a noninvasive diagnostic method and can be performed within 10 minutes by minimally skilled personnel, and without the use of laboratory equipment.
This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection withH. pylori.
TheOnSiteH. pylori Ag Rapid Test detects antigen present in the feces by using specific antibodies, which indicates an activeH. pyloriinfection. However, a negative test result does not preclude the possibility of infection withH. pylori. It can also be used to monitor the effectiveness of treatment and the recurrence of an infection, and is not affected by the use of Proton Pump Inhibitors (PPI). It is reported that the seroprevalence ofH. pyloriin specimens with positive fecal occult blood (FOB) test results is approximately 39.3%. Therefore a specimen that tests positive with an FOB test may also be tested positive with theOnSiteH. pylori Ag Rapid Test. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device.
Syphilis Cards are diagnostic test kits manufactured by Avecon Healthcare Pvt Ltd specifically for the detection of syphilis infections. These cards are designed to provide accurate and rapid results by detecting antibodies against the Treponema pallidum bacterium, the causative agent of syphilis
As we are Syphilis Rapid Test Kits manufacturer and supplier, we are specializes in providing diagnostic tools for the detection of antibodies against the Treponema pallidum bacterium, the causative agent of syphilis. These kits are designed to deliver quick and accurate results, aiding in the diagnosis and monitoring of syphilis infections.
Additional Information:
Delivery Time : 7 DAYS
NS1 tests diagnose the non-structural protein of the dengue virus. The protein that is veiled into the blood of a patient diagnosed with dengue infection. Through this test, the keen phase of the virus infection can be detected. This sensitive test can show the infection of 0-7 days. If you have attained this stage, then this test is not considered valid.
Positive NS1 result shows the presence of dengue infection in a human body but does not provide the entire information. Otherwise, serotype information is not necessary for the care of the infected person, but still this information matters.
SpecimenThese test kits are available commercially. Various laboratories and public health care centers utilize thisDENGUE NS1 Rapid Test Kit.
Additional Information:
Delivery Time : 7 DAYS
Troponin I rapid tests are diagnostic tools designed for the rapid and on-site detection of troponin I levels in a patients blood sample. These tests provide quick results, allowing for immediate assessment of cardiac health and the possibility of a heart attack.
As a Troponin I Test Kit Manufacturer and Supplier, we are specializes in producing high-quality diagnostic tools for the rapid and on-site detection of Troponin I levels in patients blood samples. These tests are designed to provide fast and accurate results, enabling healthcare professionals to quickly assess cardiac health and the possibility of a heart attack.
Additional Information:
Delivery Time : 7 DAYS
The TRUSTline HCV Ab Rapid Test provides fast, accurate results allowing users to detect infection during initial stages and take early steps to prevent serious complications and transmission.
The TRUSTline HCV Ab Rapid Test is a double antigen lateral flow chromatographic immunoassay for the qualitative detection of anti-hepatitis C virus antibodies (IgG, IgM, IgA) in human serum, plasma or whole blood.
Utilizes a Core-NS3-NS4-NS5 double antigen method
Evaluated by NIB
Highly sensitive detection of low level titre antibodies
Simple test procedure
Efficient, easy-to-interpret result
No equipment required
The OnSite H. pylori Ab Combo Rapid Test is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM and IgA) against Helicobacter pylori (H. pylori) in human serum, plasma or whole blood.
Uses serum, plasma or whole blood specimen
No need to avoid certain medications
Non-invasive, easy to perform procedure
Time to result is 15 minutes
Each Kit Contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Plastic droppers
Sample Diluent (REF SB-R0191, 5 mL/bottle)
One package insert (instruction for use)
Uses serum, plasma or whole blood specimen
No need to avoid certain medications
Non-invasive, easy to perform procedure
Time to result is 15 minutes
Each Kit Contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Plastic droppers
Sample Diluent (REF SB-R0191, 5 mL/bottle)
One package insert (instruction for use)
Uses serum, plasma or whole blood specimen
No need to avoid certain medications
Non-invasive, easy to perform procedure
Time to result is 15 minutes
Each Kit Contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Plastic droppers
Sample Diluent (REF SB-R0191, 5 mL/bottle)
One package insert (instruction for use)
Product Overview
The OnSite Chikungunya IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM anti-chikungunya (CHIK) virus in human serum, plasma or whole blood.
Uses serum, plasma or whole blood specimen
Utilizes recombinant antigen derived from the CHIK structure protein
IgM immunoassay is the most practical lab method
Distinguish from dengue infection which presents with similar symptoms
Product Overview
MERISCREEN Dengue NS1 Ag is a rapid immunochromatographic assay for detection of Dengue NS1 antigen in human serum or plasma.One Step Test For Dengue NS1 Meriscreen Dengue N1 Ag
meriscreen dengue igg/igmab is a rapid immunochromatographic assay for detection of dengue antibodies in human serum or plasma. The assay is used as a screening test for detection of dengue viral infection.
The TRUSTline HBsAg Rapid Test is highly sensitive and accurate screening test for ensuring safe blood supplies.
A lateral flow chromatographic immunoassay for the qualitative detection of hepatitis B surface antigen (HBsAg) in human serum or plasma at a level equal to or higher than 0.5 ng/mL.
Uses serum or plasma
Evaluated by NIB
Can be performed without the use of laboratory equipment
Result in 15 minutes
The TRUSTline Malaria Pf/Pv Ag Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of Plasmodium falciparum (Pf) and vivax (Pv) antigen in human blood specimen.
Meets WHO acceptance criteria
Ease of use, requires minimal training of personnel
Expanded testing facility options including areas where quality microscopy is not available
Quick turnaround time to results
Increased cost effectiveness, no high cost equipment monitoring
Availability of Positivia external controls
Product Overview
The OnSite HAV IgG/IgM Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Hepatitis A virus (HAV) in human serum, plasma or whole blood.
Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV.
Indicates protective immunity by detecting HAV IgG titers ?70 mIU/mL.
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%.
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation.
Small sample volume (5 L) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patients visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months, 2-30 C.
MERISCREEN Syphiline is a single test device for the qualitative detection of Syphilis antibodies (IgM, IgG & IgA) in Human Serum/Plasma/Whole Blood samples
Indication:
Direct & specific diagnostic methodof anti-treponema pallidum(TP) antibody
The OnSite S. Typhi/Paratyphi Ag Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of Salmonella typhi (S. typhi) and Salmonella paratyphi (S. paratyphi) antigens in human fecal specimen, serum, plasma, whole blood or blood culture specimen.
Utilizes O antigen and H antigen from both Typhi and Paratyphi serovars to maximize sensitivity
Differentiates between IgG and IgM to determine stage of infection
One step procedure minimizes operator error due to sample preparation
Test result within 15 minutes allows medical professionals to take immediate action
High level of reproducibility
Test kits can be used and stored in a wide range of temperatures
Each Kit Contains:
Individually sealed foil pouches containing:
One cassette device.
One desiccant
Stool collection devices, each containing 1 mL Fecal Sample Extraction Buffer
Plastic droppers
Patient ID stickers
Sample Diluent (1 bottle, 5 mL)
One package insert (instruction for use)
Additional Information:
Payment Terms : T/T
The OnSite S. Typhi/Paratyphi Ag Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of Salmonella typhi (S. typhi) and Salmonella paratyphi (S. paratyphi) antigens in human fecal specimen, serum, plasma, whole blood or blood culture specimen.
Utilizes O antigen and H antigen from both Typhi and Paratyphi serovars to maximize sensitivity
Differentiates between IgG and IgM to determine stage of infection
One step procedure minimizes operator error due to sample preparation
Test result within 15 minutes allows medical professionals to take immediate action
High level of reproducibility
Test kits can be used and stored in a wide range of temperatures
Each Kit Contains:
Individually sealed foil pouches containing:
One cassette device.
One desiccant
Stool collection devices, each containing 1 mL Fecal Sample Extraction Buffer
Plastic droppers
Patient ID stickers
Sample Diluent (1 bottle, 5 mL)
One package insert (instruction for use)
The OnSite Troponin I Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of cardiac Tropnin I (cTnI) and its complex in human serum, plasma or whole blood at a level equal to or higher than 1 ng/mL.
Point of Care test, suitable for emergency care
Limit of Detection (LOD) to cTnI complex of 0.3/0.5 ng/ml (S, P & WB)
LOD is calibrated by NIST standard
Can be used with serum, plasma, and whole blood.
Utilizes polyclonal and monoclonal antibody pair to reduce interference
TheTRUSTlineHIV-Ab/Ag 4thGen Rapid Test detects HIV p24 in addition to IgG and IgM, enabling HIV infection to be caught as early as 16 days post-infection.
A lateral flow immunoassay for the qualitative detection of antibodies (IgG, IgM, and IgA) to anti-HIV-1 & 2 virus and HIV-1 p24 antigen in human serum, plasma, or whole blood.
4th Generation HIV test to detect p24 in addition to IgG and IgM for early detection
Evaluated by NIB
It requires only 5 L of specimen
Use serum, plasma, or whole blood
Results are available within 15 minutes to allow prompt action to be taken at the point of care
Performance validated with BBI low-titre panel and Chinese FDA HIV-Ab Panel
The OnSite TORCH Panel Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Toxoplasma gondii (T. gondii), rubella virus, cytomegalovirus (CMV), herpes simplex virus 1 (HSV-1), and herpes simplex virus 2 (HSV-2) in human serum, plasma, or whole blood.
This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with T. gondii, rubella virus, CMV, HSV-1 and HSV-2. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device.
Recommended For Use:
Any person presenting with clinical signs or symptoms consistent with TORCH infection.
Women who are pregnant or who are planning to become pregnant
Individuals with a compromised immune system
The OnSite TORCH Panel Rapid Test detects and differentiates IgG and IgM antibodies for all 5 TORCH infections. In general, a negative test result indicates that the individual is at risk for acquiring a primary infection. A positive IgM result only indicates acute infection, a positive IgM and IgG test indicate acute, late phase infection, and a positive IgG test result only indicates past or chronic infection.
The presence of IgM anti-rubella virus or high titers of IgG anti-rubella virus (> 200 IU/mL) are suggestive of acute rubella infection. Lower titers of IgG anti-rubella virus (? 10-15 IU/mL) are suggestive of previous exposure and protective immunity. An individual with an IgG anti-rubella virus titer less than 10-15 IU/mL is considered to be at risk of acquiring a rubella virus infection.
The TORCH Panel Rapid test also differentiates between HSV-1 and HSV-2 antibodies using HSV-1 specific glycoprotein G1 and HSV-2 specific glycoprotein G2.
The TRUSTline Scrub typhus IgG/IgM Rapid Test ais a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM antibodies for Orientia tsutsugamushi (Scrub typhus) in Human Serum/ Plasma/ Whole blood specimen.
Utilizes Recombinant Orientia tsutsugamushi antigens.
Qualitative detection and differentiation of antibodies(IgG and IgM) against Orientia tsutsugamushi (Scrub typhus)
Compatible with Whole blood, Serum and Plasma.
Sensitivity: For IgG 95.4% and IgM 96.1%, Specificity: For IgG 96.8% and IgM 97.6%.
Results in 20 minutes.
Product Overview
Product Overview
Product Overview
Meriscreen HCGProduct Overview
Product Overview
Product Overview
| Method | Lateral flow Immunochromatographic Assay |
| Detection | Qualitative detection of dengue NS-1 Antigen |
| Specimen | Serum/Plasma |
| Specimen Volume | 60 l or 3 drops |
| Buffer Volume | No buffer |
| Interpretation Time | 5-20 minutes |
| Sensitivity | 96.00% |
| Specificity | 98.30% |
| Storage Temperature | 4-30 C |
| Shelf Life | 24 Month |
| Test format | Device |
| Kit Presentation | 10/30Test |
Additional Information:
Delivery Time : 7 DAYS
Troponin I rapid tests are diagnostic tools designed for the rapid and on-site detection of troponin I levels in a patients blood sample. These tests provide quick results, allowing for immediate assessment of cardiac health and the possibility of a heart attack.
As a Troponin I Test Kit Manufacturer and Supplier, we are specializes in producing high-quality diagnostic tools for the rapid and on-site detection of Troponin I levels in patients blood samples. These tests are designed to provide fast and accurate results, enabling healthcare professionals to quickly assess cardiac health and the possibility of a heart attack.
Additional Information:
Delivery Time : 7 DAYS
Dengue NS1 Antigen self-test is a rapid solid phase immune-chromatographic test for the qualitative detection of Dengue NS1 Ag in human whole blood/serum/plasma. This test is intended to be for home use with self-collected whole blood specimens from individuals aged 18 years or above( or collected by adults for individuals below 18 years of age) as well as for professional use with venous Whole blood/Serum/Plasma samples. This test is for in-vitro diagnostic use only & is designed as an aid in the early diagnosis of dengue infection patients with clinical symptoms.
Salient FeaturesAdditional Information:
Delivery Time : 7 DAYS
Scrub Typhus IgM/IgG/IgA Card is a rapid solid phase immuno-chromatographic assay for the qualitative detection of IgM, IgG& IgA antibodies to Scrub Typhus in human serum / plasma / whole blood. This test is for in vitro diagnostic use only and is intended as an aid to early diagnosis of Scrub Typhus infection in patient with clinical symptoms.
Salient FeaturesAdditional Information:
Delivery Time : 7 DAYS
Covid 19 Ag Card Test is designed for in vitro qualitative detection of Covid 19 antigen in human nasopharyngeal, nasal swab specimens. The kit is intended for professional use and as a screening test and is an aid in early diagnosis of SARS COV-2 infection in patients with clinical symptoms.
Salient FeaturesRapid Visual Test for the Qualitative Detection of Covid-19 (SARS-COV-2) antigen in Human nasopharyngeal and nasal swab specimens.
Additional Information:
Delivery Time : 7 DAYS
HIV testing or screening is done to get to know the presence of the virus in the human body. There are a number of tests that can be done to check your blood if you are infected with the HIV virus. Not all tests can detect this virus in your body as it takes time for the virus to grow in your body.
The consequence of HIV testing:If your body has the virus and it gets detected at an early stage, then the treatment can be started and the growth of that virus can be stopped right there.
Who should get this test done?Nowadays the awareness of this test is at high and thus the usage ofHIV rapid test kitis increasing at a high speed. This kit can offer you results within 5 to 15 minutes and the results are 99% accurate. Medical practitioners totally rely on this kit to detect this virus.
Additional Information:
Delivery Time : 7 DAYS
The OnSite Typhoid IgG/IgM2.0 Rapid Test is a lateral flow immunoassay for the qualitative detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum or plasma.
Utilizes O antigen and H antigen from both Typhi and Paratyphi serovars to maximize sensitivity
Differentiates between IgG and IgM to determine stage of infection
One step procedure minimizes operator error due to sample preparation
Test result within 15 minutes allows medical professionals to take immediate action
High level of reproducibility
Test kits can be used and stored in a wide range of temperatures
Each Kit Contains:
Individually sealed foil pouches containing:
One cassette device.
One desiccant
Plastic droppers
Sample Diluent (1 bottle, 5 mL)
Additional Information:
Delivery Time : 10 Days
Additional Information:
Delivery Time : 7 DAYS
Additional Information:
Delivery Time : 7 DAYS
Oscar Syphilis Card test is intended used for qualitative detection of antibodies (IgM/IgG/IgA) of Treponema pallidum (TP) in human serum / plasma as in aid of Syphilis diagnosis. It is for in-vitro diagnostic use only. The test is based upon immuno-chromatographic principle. Recombinant proteins of TP have been used in the test formulation to make it highly sensitive and specific. Serum / plasma can be used for testing. No buffer & no dilution of sample are required for performing the test. Oscar Syphilis Card test has shelf life of 24 months from date of manufacturing if stored at 2-30°C under sealed condition. Each kit of Oscar Syphilis Card test contains 50 pcs of individually sealed pouches containing test cards and disposable sample dropper. Test can be performed using two-three drops of serum / plasma and result can be read within 5-10 minutes.
hiv ag & ab card (4th generation) is a visual, rapid qualitative and sensitive solid phaseimmunochromatographic assay for the differential detection of hiv-1 p24 antigen and antibodies (igm, igg &iga) to hiv-1& hiv-2 in human serum/ plasma/ whole blood (collected by venipuncture or fingerprick). thetest is a screening test for p24 antigen (hiv-1) and hiv antibodies (anti-hiv-1 & anti-hiv-2) and is for in vitrodiagnostic use only. it is intended for screening of blood donors or other individuals at risk for hiv-1 & hiv-2infection and for clinical diagnostic testing. it is a screening test for p24 antigen (hiv-1) and hiv antibodies(anti-hiv-1 & anti-hiv-2). the test is for in vitro diagnostic use only and is intended for screening of blooddonors or others individuals at risk for hiv-1 and/or hiv-2 infection and for clinical diagnostic testing.
salient featuresfinger prick, rapid, visual and qualitative immunoassay.4th generation rapid test for differential detection of p24 antigen & antibodies for hiv in serum/plasma /whole blood.ideal for blood screening, detects sero-negative hiv cases.use of gp-41, c terminus of gp120 for hiv-1 , gp-36 for hiv -2 antibodies and anti-p24 for hiv p24 ag detection.detection of group 0 & subtype c of hiv-1, which is most prevalent in india.based on immunochromatography technique.see through device for easy interpretation of results.sensitivity : 100 % & specificity: 100%analytical sensitivity of hiv p24 ag : 100 iu/ml (traceable to p24 antigen nibsc standard, u.k. code no. 90/636)long shelf life 30 months at 2-30cconvenient pack size: 25 t.
Additional Information:
Delivery Time : 7 DAYS
Additional Information:
Delivery Time : 7 DAYS
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Delivery Time : 7 DAYS
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Delivery Time : 7 DAYS
Mr. Raj Bhupender (Raj Biosis Private Limited)
F-1, Plot No. 16, D-Block, Satya Colony, Tagore Nagar On 200 Feet, Ajmer Jaipur Expressway, Rajasthan - 302021, India
https://www.indianbiomedicals.com
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