Cellife Home Test Exw
Cellife home test is approved by Australia TGA Standard
Order: 50% deposit/balance Exw
Lead time: around 7-10days
Sometimes will have Extra OTG China
You can got the approval for sale in Australia
And Cellife distributor (none sole) in Australia will help you to Customs clearance
***FOR USA BASED END-CLIENTS ONLY***
300 PER CASE; 20 CASES / 6,000 PER PALLET; 40 X 48 72 280kgs
Bulk orders placed this week will start to deliver on/about early March with partial weekly shipments.
*Terms of sale reflect those of ACON LABS; 50% deposit; balance when goods are ready to start shipping from LA
*Full pre-payment will move you up to the front and expedite quicker shipment considerations.
* Delivery is subject to final confirmation
#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
5093 Diagnostic Kits Suppliers
Short on time? Let Diagnostic Kits sellers contact you.
dear my friend, we are from Lepu Medical, the manufacturer for the self testing kits.
we are offering the goods will CE and also very fast production time.
Starting from the IVD test, our products now is hot welcomed in the world.
You may freely contact with us in the WhatsApp 008613230113351
or maybe the email address at dannis.wen@lepu-medical.com
we are opening for the worldwide buyers to have the goods.
If you need, you can also find our in our web or Alibaba.
We are willing to meet and make new friends around the world.
PRoduct Name :
Sars cov 2 (covid 19) igg/igm rapid test cassette
Product Description :
The ACtest COVID-19 IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG antinCoV-19 virus and IgM anti-nCoV-19 virus in human whole blood, serum or plasma. It is intended to be used by professionals as a screening test and as an aid in the diagnosis of infection with nCoV-19 viruses. The product has obtained the CE certification and is on the list of government export permits. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries.
Price of product ( USD price or FOB price) :
USD 3.5- USD 5 per test
Product origin :
Hangzhouï¼?Zhejiangï¼?China
Key Specifications/Special Features :
"
Place of OriginHangzhouï¼?Zhejiangï¼?China
Port Of Loading Shanghai
Payment Term T/T
Delivery Time Shipment within 7 working "
Minimum Order Size and Packaging details
Packing 40test/box, 25box/carton ,Minimum Order Quantity 1000test
I am the manufacturer of COVID-19 RAPID TEST in China. The ACtest COVID-19 IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-nCoV-19 virus in human whole blood, serum or plasma. It is intended to be used by the professionals as a screening test and as an aid in the diagnosis of infection with nCoV-19 viruses. The product has obtained the CE certification and is on the list of government export permits. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries.
We are a manufacturer of SARSCoV2 RAPID TEST CASSETTE in China. We can provide customers following SARSCoV2 rapid testing products that have obtained the CE or other certifications. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries.
SARSCoV2 IgG/IgM Rapid Test Cassette
SARSCoV2 Antigen Rapid Test (nasopharyngeal swab)
SARSCoV2 Antigen Rapid Test (Saliva)
SARSCoV2 and Influenza A+B Antigen Combo Rapid Test
SARSCoV2 Neutralizing Antibody Test Kit
We are a manufacturer of SARSCoV2 RAPID TEST CASSETTE in China. We can provide customers following SARSCoV2 rapid testing products that have obtained the CE or other certifications. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries.
SARSCoV2 IgG/IgM Rapid Test Cassette;
SARSCoV2 Antigen Rapid Test (nasopharyngeal swab);
SARSCoV2 Antigen Rapid Test (Saliva);
SARSCoV2 and Influenza A+B Antigen Combo Rapid Test;
1. PROTAN COVID-19 IgM/IgG
Protan Covid-19 IgM/ IgG is In-Vitro kit for the qualitative measurement of anti-COVID-19 IgM and IgG antibodies in human whole blood, plasma, and serum which non-medical professionals can use.
It produces results in 15 minutes without additional analyzer and is for easy, simple and rapid test just with finger tip blood.
2. PROTAN COVID-19 IgG Type2
In-Vitro kit for the qualitative measurement of SARS-Cov-2 IgG antibodies against SP-RBD in human whole blood, plasma, and serum.
Protan Covid-19 IgG Type2 neutralizing Antibody Rapid Test Kit is to check whether the formation of Covid-19 Neutralizing antibodies After vaccination.
Protan Covid-19 IgG Type2 is intended for the detection of neutralizing antibodies(IgG) against Covid-19 SP RBD(spike protein-receptor binding domain) in Human whole blood after vaccination.
This kit is only used for the in vitro qualitative detection of 2019-nCoV antigen from
human nasopharyngeal swab, nasal swab or oropharyngeal swab specimens.
This kit is suitable for the auxiliary diagnosis of COVID-19, the results are for clinical
reference only and cannot be used as the sole basis for diagnosis and exclusion
decision. The clinical diagnosis and treatment of patients should be considered in
combination with their symptoms/signs, medical history, other laboratory tests and
treatment responses.
Positive test result needs to be further confirmed, negative result does not preclude
2019-nCoV infection.
This kit is intended for use by qualified and trained clinical laboratory personnel
specifically instructed and trained in the techniques of in vitro diagnostic procedures.
TEST PRINCIPLE
The kit is immunochromatographic and uses double-antibody sandwich method to
detect 2019-nCoV N protein antigen. During detection, the treated specimens are
loaded into the sample wells of the test card. When the concentration of 2019-nCoV
antigen in specimen is higher than the minimum detection limit, the viral antigen will
form complexes with labeled antibodies first. Under chromatography, the complexes
move forward along the nitrocellulose membrane till captured by pre-coated
monoclonal antibody of 2019-nCoV in detection zone on nitrocellulose film (T) to
form a pink/purple reaction line on the detection zone, at this point the result is
positive; conversely, if there is no viral antigen or the concentration of antigen in
specimen is below the minimum detection limit, no pink/purple reaction line appears
in the detection zone, at this point the result is negative. Regardless of whether the
sample contains viral antigens or not, a pink/purple reaction line will appear in the
quality control zone (C), the pink/purple reaction line that appears in the quality
control zone (C) is the criterion for determining if the chromatography process is
normal.
