Watmind COVID-19 / SARS-COV-2 Antigen Rapid Test / Lolly Test, Approval for Private Use / Self-administration by Lay Persons, File Number Special Approval 5640-S-032/21 Bfarm: AT108/20 – BfArM Listing (reimbursable) – PEI evaluated (1 test per box)

Covid-19 Saliva Test from Watmind

Most rapid corona antigen tests require a swab in the nose or posterior nasopharynx. For many test subjects, this form of specimen collection is very uncomfortable or even painful. Children and seniors are particularly sensitive in the nose or throat. A saliva test such as the Watmind lay test is the gentle and painless alternative. This Lollitest is non-invasive and is suitable for people of all ages.

If you are responsible for a daycare center or elementary school, this lay test is a suitable product. It helps ensure infection control in your facility. Staff and children can test regularly and without complications. This makes it easier to maintain attendance. However, the Lollitest is also suitable for use in retirement and nursing homes or facilities for people with disabilities.

How the Watmind lay test works

Sample collection is easy even for young children with a little assistance. To perform the saliva test, the sterile swab provided must be soaked with saliva for at least 10 seconds under the tongue. In doing so, it should be rotated at least five times. To obtain a reliable result, the swab must be completely saturated with saliva fluid. In addition, no food or drink should be consumed 30 minutes before the sample is taken.

Once the swab is completely saturated with saliva, it is dipped into the test tube containing the extraction fluid. The swab must be turned over several times and thoroughly squeezed against the walls of the tube as it is pulled out. This ensures that a maximum of the saliva sample is available. A few drops of the solution are then added to the test cassette. After about 15 minutes, the test result can be read.

BfArM-tested quality

The Watmind Lollitest is listed with the BfArM and has special approval as a lay test. It has a sensitivity of 95.51% and a specificity of 99.45%. In addition, it also detects viral mutations. When stored between 4 and 30° Celsius, the Watmind lay test can be used for 18 months.

The saliva test comes in a pack of 1. Each pack of 1 contains

• 1 test cassette
• 1 sterile swab
• 1 extraction tube with buffer liquid
• 1 disposal bag
• 1 instruction manual

Details:

• Sensitivity: 95.51 %
• Specificity: 99.45 %
• BfArM listed (AT108/20)
• PEI evaluation
• Duration: approx. 15 minutes
• Storage temperature: 4 – 30°C
• Lay test approved! (File number of the special approval of the BfArM: 5640-S-032/21)

Use the Watmind lay test to give your staff and visitors to your business or facility a sense of safety. The sooner infected individuals are identified, the sooner chains of infection can be broken and the spread of Corona virus prevented. In addition, regular testing will ensure the smooth running of your operation.

This is PPE Partner

We are your wholesale and specialized dealer when it comes to high quality Personal Protective Equipment and certified Corona antigen rapid tests. You can count on us for fast delivery and fair pricing. Please note that minimum order quantities apply to all of our items. If you have any questions about a product, please contact our customer service team.

Please note:

This offer for a Corona Rapid Test is intended exclusively for commercial customers (physicians, healthcare professionals, companies) with appropriate professional staff. This product is not a layman’s test that may be ordered by private individuals – the purchase of this Corona rapid test is strictly defined according to the Medical Devices Dispensing Ordinance §3.

!!! You confirm with your purchase that you are placing the order for commercial/medical purposes and you are handing over the products to appropriate qualified personnel. Therefore, each order will be carefully checked! Please understand that we unfortunately have to cancel your order if you can not provide proof that you are an authorized person according to MPAV !!!

Note for companies

As a result of an amendment to the Medical Devices Dispensing Ordinance (MPAV), as of February 2, 2021, companies and institutions that provide a service to the general public, the failure or impairment of which would lead to significant supply shortages or endanger public safety, may also obtain and use rapid antigen tests for the detection of the coronavirus SARS-CoV-2.

This means that you are an authorized person under the MPAV.

In concrete terms, this means that these companies and facilities can offer regular testing for their employees and visitors and make these tests part of their hygiene and protection concept, ideally with advice from the respective company medical service or the employers’ liability insurance association.

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