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HomeProductsCOVID-19 ProductsRapid Test AntigenFlu A & Flu B & COVID-19 Ag Rapid Test Single-strand RNA Viruses Sars-CoV-2 Antigen Membrane RBD
Flu A & Flu B & COVID-19 Ag Rapid Test Single-strand RNA Viruses Sars-CoV-2 Antigen Membrane RBD
Flu A & Flu B & COVID-19 Ag Rapid Test Single-strand RNA Viruses Sars-CoV-2 Antigen Membrane RBD
Flu A & Flu B & COVID-19 Ag Rapid Test Single-strand RNA Viruses Sars-CoV-2 Antigen Membrane RBD
  • Flu A & Flu B & COVID-19 Ag Rapid Test Single-strand RNA Viruses Sars-CoV-2 Antigen Membrane RBD
  • Flu A & Flu B & COVID-19 Ag Rapid Test Single-strand RNA Viruses Sars-CoV-2 Antigen Membrane RBD
  • Flu A & Flu B & COVID-19 Ag Rapid Test Single-strand RNA Viruses Sars-CoV-2 Antigen Membrane RBD

Flu A & Flu B & COVID-19 Ag Rapid Test Single-strand RNA Viruses Sars-CoV-2 Antigen Membrane RBD

    Payment Type: L/C,T/T,Money Gram,Western Union
    Incoterm: FOB,EXW,FCA,CPT,CIP
    Min. Order: 1000 Piece/Pieces
    Delivery Time: 15 Days

Basic Info

Types of: Blood Analysis SYstem

place of origin: China

Medical device classification: Class I

Warranty Service: 1 Year

After-sales service: Online technical support

Additional Info

Packaging: box/carton

Productivity: 50000 PCS/Day

Brand: Poweray

Transportation: Ocean,Air,Express

Place of Origin: China

Supply Ability: 300000 PCS/Week

Certificate: ISO 13485-2016

Port: Hong Kong,Shenzhen

Product Description

Product introduction:

The Novel Coronavirus (COVID-19) Antibody IgM/IgG Test developed by Bioda uses colloidal gold immunochromatography technology and capture method to detect (COVID-19) IgM/IgG antibody in human body, which is used for the qualitative test of (COVID-19) IgM/IgG antibodies in human serum, plasma and venous whole blood samples in vitro. The test results will be observed with the naked eye after about 15 minutes. It can be used as a supplementary test indicator for suspected cases whose COVID-19 nucleic acid tests show negative or used in conjunction with nucleic acid tests in the diagnosis of suspected cases.


Reaction time: 15min
Blood sampling method: peripheral blood or venous blood

Features
STORAGE INSTRUCTIONS:
1. Store at room temperature (2-30ºC or 35.6-86°F) in a dry place. Avoid direct sunlight;
2. 18 months of shelf life (date of manufacture to expiration date).
Specimen collection
A) Nasal Aspiration
Collect nasal aspirate fluids using the specific aspirate as instructed.
B) Nasal Swabbing
Completely insert the sterilized swab, which is supplied in this kit into the nasal basin, and swab
several times to collect the epidermal cells of mucus.
C) Throat Swabbing
Insert the sterilized swab deep into the throat and swab several times to collect the epidermal cells of the
mucus. Contamination of the swab with saliva should be avoided.
Specimen extraction
Add 0.5 ml or 0.5-1.0 ml of the extraction solution into an extraction tube which is supplied in this kit,
and put it on the stand.
A) Nasal Wash/Aspirate
Add 0.5ml of the nasal aspirate fluid to 2ml of transfer buffer or physiological saline. Then add 0.5ml of
this mixture to the extraction tube which contains 0.5 ml of the extraction solution, and mix well by
squeezing. The extraction mixture will be used as test sample.
B) Nasal or Throat swabs
Place the swab used to collect the sample into an extraction tube which contains 0.5-1.0 ml of the
extraction solution, and immerse the swab by squeezing the tube several times. Remove the swab and use
the extraction mixture as test sample.
TEST PROCEDURE:
Step 1 Bring the test to room temperature (18-26ºC) before use.
Step 2 Open the foil pouch, take out the test and lay it on an even surface.
Step 3 Add 3 drops(about 100 µL )of extraction mixture into the each sample well (S).
Step 4 Read and record the results at 15 minutes after addition of samples.


QUALITY CONTROL:

It is recommended to use control samples. The use of control samples is advised to assure the day to day
validity of results. Use controls at both normal and pathological levels.
It is also recommended to make use of national or international Quality Assessment programs in order to
ensure the accuracy of the results.
Employ appropriate statistical methods for analyzing control values and trends. If the results of the assay
do not fit to established acceptable ranges of control materials patients results should be considered
invalid. In this case, please check the following technical areas: Pipetting and timing devices; expiration
dates of reagents, the specimen collection procedure and storage conditions.

Specimen swab ag rapid test

Img 97432110


FAQ:
Q1: Why choose us?
Poweray is located in Shenzhen Pingshan National Bioengineering Base. Both OEM and ODM are available besides sampling tube products, L/T is accurate and same quality control standard per sample confirmed.
Q2: Order processing
MOQ and customized factors confirmed. Exporting and Importing certificates verified. Firm shipping schedule on deposit with PO.
Q3: VTM Specimen Collection
Wearing medical protective clothing and gloves to keep sterile operation is important and prerequisite. Following standard sampling kits setting and operating instructions to collect good nas safely. Washing gloves put on the hands if necessary during collection schedule.

Looking for ideal Test Membrane Manufacturer & supplier ? We have a wide selection at great prices to help you get creative. All the Sars-CoV-2 Antigen are quality guaranteed. We are China Origin Factory of RNA Viruses. If you have any question, please feel free to contact us.

Product Categories : COVID-19 Products > Rapid Test Antigen

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