Find Verified Covid 19 Detection Kit Suppliers, Manufacturers and Wholesalers

Controller Tubing Assembly
01 unit SCD700
01 pair COVIDIEN 9729
01 box COVIDIEN 9728

GOOD EXPIRATION DATE

New: BRAND NEW , unused, unopened, undamaged item in its original packaging (where packaging is applicable). Packaging should be the same as what is found in a retail store, unless the item was packaged by the manufacturer in non-retail packaging, such as an unprinted box or plastic bag. See the seller's listing for full details

Policy
This item is being sold "AS-IS" but guaranteed to be as pictured and described. We make every effort to describe each item as best as we can and we ask that you please read the listing in its entirety. Buyers are responsible for knowing the functional operation and final testing prior to implementing for service.

Payment Terms
We accept payment only through PayPal.

Refunds
Refunds will be issued within 14 business days after the receipt of the equipment. All returned items must be in original condition, packaging, sealed and unused, tamper tag must be intact. We reserve the right to reject the item after inspection, (items with physical damage or incomplete packaging, incomplete items). In the event that physical damage is caused during transit of a return, it is the customers�??�?�¢?? responsibility to contact the carrier to start a damage claim upon receiving a notification from us. The responsibility is between the customer and the carrier.

Shipping Terms
Items ship within 1-2 business days after payment is received. Items will not ship on Saturday and Sunday. Orders will be shipped by the most cost effective channel. All items are packaged and shipped in a professional manner. The tracking number will be sent to you. Combined shipping discounts are available for multiple item purchases. Flat rate fees are for Continental US shipping ONLY. Alaska, Hawaii and all other NON Contiguous Territories are extra cost.

Return Policy
Items are sold as-is with no returns or refunds available unless explicitly stated.

Covid 19 detection kit, famous for efficient detection of Covid 19/coronaVirus
made in south korea

Both COVID-19 and influenza A/B viruses (Flu A/B) can cause acute respiratory infections, and people are generally susceptible. These three viruses are highly contagious, spread quickly, have a short incubation period, and have a high incidence. Symptoms of COVID-19 and influenza may look similar; the main symptoms include fever, dry cough, fatigue, etc. With this combination test, healthcare workers can provide an accurate diagnosis to patients and treat them with the appropriate measures.

Feature
Results ready in 15 minutes
Accurate diagnostic tool for active infection
Easy to administer and read results
Affordable, no need for instrument, highly portable
Enable testing on a massive scale
For healthcare workers use only

To help stop the spread of COVID-19, Singclean Medical has developed COVID-19 Antigen Test Kits saliva swab which is a solid phase immunochromatographic assay for the rapid, qualitative detection of antigen from COVID-19 in human saliva swab specimen. The test provides only a preliminary test result. Therefore, any reactive specimen with the COVID-19 Antigen Test kit (Colloidal Gold) must be confirmed with alternative testing method (s) and clinical findings.

Advantage:
Quick: results ready in 15 minutes
Affordable: no need for instrument
Accurate diagnostic tool for active infection
Easy to administer and read results
Enable testing on a massive scale
Non-invasive: more comfortable than nasopharyngeal swab




Warnings
1. Use fresh samples whenever possible.
2. Positive results do not rule out bacterial infection or co-infection with other viruses.
3. A negative result can occur if the quantity of the COVID-19 antigen present in the specimen is below the detection limits of the assay, or failed to collect the COVID-19 antigen.
4. Negative results do not rule out infection with COVID-19 and should not be used as the final or sole basis for treatment or patient management decisions. Negative results should be considered in the context of a patientâ??s recent exposures, history and the presence of clinical signs and symptoms consistent with COVID-19. For a more accurate test result, repeat the tests or confirmed with other testing methods and clinical findings is recommended

CE Approved Covid-19 IgG/IgM Antibody Blood Test Kit can be used as an initial screening for qualitative and differential detection. Throughout testing the antibody of IgG and IgM immunoglobulins in human serum, plasma or blood, the test kit can show the result in a short time.
Relative sensitivity 96.00%(192/200)
Relative specificity 98.29%(806/820)
Accuracy 97.84% (998/1020)

Advantages
Fast detection: 10 minutes to interpret the result;
Easy to operate: no complex equipment required during test;
Sensitive: the product has a higher sensitivity than PCR Nucleic Acid

Global Network
Singclean@COVID-19 lgG/gM Test Kit has been sold to more than 50 countries in the worid, like Brazil, Chie,Polandï¼?spain, Bolivia, Greece, Lihuania, Ecuador, Ukraine and Turkey.

Precaution
It is worth noting that the result of Covid-19 IgG/IgM antibody blood test should not be used as the only evidence of Coronavirus diagnosis. Professional doctors and clinical findings are necessary if the result of antibody test is positive. Besides, the test kit should be operated by professionals only. Use by individuals may cause deviation in test results.

Limitation
False negative and false positive could happen. If the antibody is lower than the detection level, especially in the 7 days of the onset of symptoms, a positive patient may also be diagnosed as negative.

CE Approved Singclean COVID-19Test Kit (Colloidal Gold Method) is a solid phase immunochromatographic assay for the rapid,qualitative detection of antigen from COVID-19 in human nasal swab specimen.This test provides only a preliminarytest result. Therefore, any reactive specimen with the COVID-19 Test Kit (Colloidal Gold Method) must be confimed with alternative testing method(s) and clinical findings.

This rapid antigen test kit is the second test kit developed by Singclean Medical for COVID-19 testing on the basis of Colloidal Gold Method after Singclean COVID-19 lgG/IgM Test Kit, an antibody test, was launched globally in March.

Advantage
Results ready in 15 minutes
Accurate diagnostic tool for active infection
Easy to administer and read results
Affordable, no need for instrument, highly portable
Enable testing on a massive scale
For healthcare workers use only


Sensitivity 98.56%
Sensitivity 99.03%
Accuracy 98.84%

Warnings
1. This test is not for at home testing, and should only be operated by healthcare workers.
2. Optimal assay performance requires strict adherence to the assay procedure described in this insert sheet. Inadequate or inappropriate sample collection, storage, and transport may cause false test results.

Korean made Gmate COVID-19 Saliva Antigen Test Kit is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human saliva specimens. This test is an aid to early diagnosis of SARS-CoV-2 infection in patients with clinical symptoms with SARS-CoV-2 infection.
â?¢ 90.9% Sensitivity, 100% Specificity
â?¢ Made in Korea
â?¢ Easy to Use
â?¢ Currently the only imported brand approved and fully registered with governments and medical / health agencies for professional and home use.
Provides initial screening result only
Disclaimer: Reactive specimens must be confirmed with alternative testing method(s)

We Supple Grade A medical examination Disposable Covid-19 test kit and Syringes with affordable prices in major international market free to contact us for more Quotation.

The COVID-19 IgG/IgM (Whole Blood/Serum/Plasma) Rapid Test Device utilizes lateral flow technology that is used for the qualitative, differential detection of both anti-SARS-CoV-2 IgM and IgG antibodies. In general, antibodies can be detected 1-3 weeks after infection. This test is intended to screen patients for COVID-19. Combining RNA and Antibody tests can significantly raise the sensitivity for detecting COVID-19 in infected individuals.

This test has been authorized by the FDA under a EUA for professional use CLIA and CLIA WAIVED for Point Of Care.
This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens.

This product is intended for professional use and not for home use.

FACT SHEET FOR HEALTHCARE PROVIDERS

This test has been authorized by the FDA under a EUA for use by authorized CLIA laboratories. This device is CLIA waived for point of care use for fingerstick whole blood specimens only. The user should be trained in the procedure. Wear appropriate protective attire for your safety when handling patient samples.
This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens.
There should be a blue line in the control region (next to ) before testing, discard the device if there is no blue line.

Due to contractual obligations to the federal government, Current suppliers have increased costs and limited production of all point of care tests without notice. We have great news! To shield our customers from excessive price increases as well as provide immediate availability, we have secured multiple FDA EUA rapid antigen test kit options. These tests have similar and/or better accuracy along with individual buffer bottles. We are currently able to provide three options: Clarity-Sienna, Indicaid and Celltrion DiaTrust kits. We work directly with the distributor and can supply by the pallet or case with pricing as low as $6.00 per kit.

CLIA Waived

Use of this test with all authorized specimen types is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet requirements to perform moderate or high complexity tests.

This test is also authorized for use with fingerstick whole blood specimens only at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.

The CLIA Waived COVID-19 IgG/IgM Rapid Test Device is an in vitro immunoassay for the direct and qualitative detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood, serum, or plasma. The test is for professional use only.

Indication:

Qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA), serum, or plasma (sodium EDTA). Intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. Emergency use of this test is limited to authorized laboratories.

About Test Device

EUA Authorized
CE Mark
Test does NOT give positive or negative result for COVID-19 virus. This is an antibody test, it only indicates past or recent infection.
Read Results in 15 Minutes
9 Month Expiration from Date of Manufacture
Contents

20 Test Devices
20 Disposable Pipettes
20 Alcohol Prep Pads
Sterile Safety Lancets
Buffer
Package Insert

The CareStart COVID-19 Antigen Test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals who are either suspected of COVID-19 by their healthcare provider within the first five days of symptom onset or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between tests.

Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet the requirements to perform moderate, high, or waived complexity tests. This test is authorized for use at the Point of Care (POC), i.e., inpatient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.

Lateral flow assay
Detect SARS-CoV-2 nucleocapsid protein antigen
Rapid results within 10-15 minutes
Intended at POC setting (i.e., in patient care settings) by medical professionals operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation
For use under the Emergency Use Authorization (EUA) only
For in vitro diagnostic use only
For prescription use only
For use with direct anterior nasal and nasopharyngeal swab specimens
Clinical Performance

93.75% PPAa and 99.32% NPAb when used with nasopharyngeal swab

87.18% PPAa and 100% NPAb when used with anterior nasal swab

Master Carton - Contains 625 Tests

For International Sale Only - Call for Pricing

The COVID-19 IgG/IgM Rapid Test Device is an in vitro Immunoassay for the direct and qualitative detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood, serum, or plasma. The test is for professional use only.

Indication:

Qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA), serum, or plasma (sodium EDTA). Intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection.

About Test Device

Gives Positive or Negative Result for COVID-19 IgM/IgG antibodies
Read Results in 15 Minutes
Contents of each box

25 Test Devices
25 Disposable Pipettes
25 Alcohol Prep Pads
Sterile Safety Lancets
Buffer
Package Insert

STANDARD M nCoV Real-Time Detection kit is used for rapid identification and detection of novel coronavirus (2019-nCoV) nucleic acids in human nasopharyngeal swabs and throat swab samples.
- One tube reaction for identification and detection of 2019-nCoV
- One-step Real-Time RT-PCR
- Provide all reagents required for PCR
- Designed according to WHO interim guidance for laboratory testing for 2019 novel coronavirus (2019-nCoV) in humans"
- nCoV primers/probes ORF1ab (RdRp) gene, E gene
Provide Internal controls


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PPE COVID home test kit supply to worldwide.
Shipping: CIF
Payment: L/C
MOQ: 100,000pcs

Access Bio
Covid 19
Antigen Test Kit
Care Start

The CareStart COVID-19 Antigen Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from symptomatic individuals who are suspected of COVID-19 by their healthcare providers.

SARS-CoV-2 Antigen Detection Kit
For Nasal Swab, home testing
Colloidal Gold Method

Package Available: 1 Test/box, 5 Tests/box, 10 Tests/box, 20 Tests/box
Carton Size: 63 x 39 x39cm
Price is different based on QTY from 10K to 500K or above
Payment Term: T/T
Delivery time: 3-5 days
Price Valid: 30 days
Quality Warranty: 2 years.

COVID ANTIGEN TEST -ROCHE
Boxes of 5 tests
Offer: 27 usd (kit with 5 tests)
6000 boxes available