Reagent Kit Cobas Liat Molecular Diagnostic / Real Time RT-PCR SARS-CoV-2 & Influenza A / B For use on the Cobas Liat System 20 tests
UOM: 20/KT
Product Number: 09211101190
Manufacturer: Roche
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On May 27th, 2022, Boson Rapid SARS-CoV-2 Antigen Test Card (Self-Testing) was authorized for marketing by Health Canada.Global Technology Foundation is a fully authorized independent distributor of Boson Biotechnology Co., Ltd. throughout North America. It has the ability to supply government and private buyers with a monthly supply of 30-40 million boxes. The quotation on this page is only for the USA .Sales, OTG supply, accept TT payment.The BOSONTM� Rapid SARS-CoV-2 Antigen Test Card (Home Test) has been sold to Europe, Southeast Asia, Australia, Canada and other countries, with excellent product quality and service. The test gained substantial popularity among users.
The only supplier with the lowest price in North America for COVID-19 antigen test kits
The US Food and Drug Administration (FDA) granted Emergency Use Authorization for the BOSONTM Rapid SARS-CoV-2 Antigen Test Card (Home Test) on April 6, 2022.
Global Technology Foundation is a fully authorized independent distributor of Boson Biotechnology Co., Ltd. throughout North America. It has the ability to supply government and private buyers with a monthly supply of 30-40 million boxes. The quotation on this page is only for the USA .Sales, DDP supply, accept TT payment.The BOSONTM� Rapid SARS-CoV-2 Antigen Test Card (Home Test) has been sold to Europe, Southeast Asia, Australia, Canada and other countries, with excellent product quality and service.  The test gained substantial popularity among users
#1) ICPO, POF-
Then fully financed, we move the product here and buyer must pay within 24hrs after it arrives CIF (Inspect and Pay)
$7.89 - add comms
CIF USA : Within 6 working days all packages will be arrived by air freight
or
#2) PAYMENT TERM
PO , 50% after PO / 50% after BOL is provided.
CIF USA : Within 6 working days all packages will be arrived by air freight
$6.89 - add comms
PO: Ruben L Hudson
Advanced Healthcare Resources LLC
c/o STM Bio - Goldmanifestor
CE Approved MAU is a rapid visual immune-assay for the qualitative, presumptive detection of albumin in urine for self-testing. The test used as a supplementary method in the diagnosis of diabetic nephropathy and other renal damage. MAU occurs when the kidney leaks small amounts of albumin into the urine.
The first indicator of a renal dysfunction, especially for diabetic patients
Independent risk indicator to evaluate the profession of chronic kidney disease (CKD).
Bacterial Vaginosis Quick Test Kit is designed as a simple, rapid, cost effective method for in vitro testing. It is qualitative test for the determination of neuraminidase (SNa) in female vaginal fluid, which is auxiliary diagnosis of bacterial vaginosis.
Application
Used to assist the diagnostic of bacterial vaginosis, evaluate the micro ecological balance in genital tract, and to prevent recurrences of vaginosis.
Advantage
High sensitivity, strong specificity
Easy operation, convenient and effective
No need of special instrument, no need of professional training
CE Approved The Follicle Stimulating Hormone (FSH) Test Kit is a rapid qualitative test for detect FSH in urine. This help to check the function of the pituitary gland and check if hormone levels are normal. The test can be used to see if a woman has started the menopause. The test may also be used (along with other tests) for detecting possible causes of both male and female infertility.
Self-detection of ovarian function
Guide to prevention of premature ovarian
Diagnosis of menopause
CE Approved The Luteinizing Hormone(LH) Ovulation Test Kit is a rapid, visual, and one-step test for the qualitative determination of LH surge in human urine specimens, to help predict ovulation time, signaling that ovulation is likely to occur in the next 24-48 hours, so as to guide reproductive women to choose the optimal conception time or safe period contraception.
Specification
This test kit is divided into three types. The specific specifications are as follows:
Strip: 1 test/box; 5 tests/box; 25 tests/box; 25T/Canister; 50 tests/box
Cassata: 1 test/box; 5 tests/box; 25 tests/box; 50 tests/box
Midstream: 1 test/box; 20 tests/box
Advantage:
Simple to use, no need for additional equipment, qualitative result in 2-5 minutes
10-25mlU/mL sensitivity
Over 99% accuracy
OEM service
CE Approved The human Chorionic Gonadotropin (HCG) Pregnancy Test Kit is a rapid, one-strip lateral flow immunoassay for the qualitative determination of HCG in human urine specimens, to aid in the early detection of pregnancy.
Advantage:
Simple to use, no need for additional equipment, qualitative result in 2-5 minutes
10-25mlU/mL sensitivity
Over 99% accuracy
OEM service
Covid-19 Antibody IgM/IgG Rapid Test kit,
Using whole blood, Serum, Plasma sample, take less than 10 minutes,
a lateral flow immunochromatographic assay for detaction of SAR-CoV-2 IgM/IgG
antibodies in human blood specimens.
Package Unit: 25 tests/kit
25 test devices
1 Assay buffer
25 blood transfer pipettes
COVID-19 IgG/IgM Rapid Antibody Test Kit with EUA FDA approval. Available immediately!
(Whole Blood/Serum/Plasma) is a solid phase immuno chromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to 2019 Novel Coronavirus in human whole blood, serum or plasma.
- Fast results as soon as 2-10 minutes
- Facilitates patient treatment decisions quickly
- Simple, time-saving procedure
- Little specimens, only 5L of serum/plasma or 10L of whole blood specimens
- All necessary reagents provided & no equipment needed
- High sensitivity and specificity
- Sensitivity: IgG 97.2%; IgM 87.9%
- Specificity: IgG 100%; IgM 100%
- Specimen: Whole Blood, Serum, Plasma
- Shelf Life: 24 months from the date of manufacture
The Coronavirus Ag Rapid Test Cassette (Swab) is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP) swab specimens directly or after the swabs have been added to viral transport media from individuals who are suspected of COVID-19 by their healthcare provider. It is intended to aid in the rapid diagnosis of SARS-CoV-2 infections. The Coronavirus Ag Rapid Test Cassette (Swab) does not differentiate between SARS-CoV and
SARS-CoV-2.
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