COVID-19 Antigen Lay Test Rapid Test Wondfo® - BfArM: AT011/20 - BfArM Listing (reimbursable) - Special Approval 5640-S-179/21 - PEI evaluated - (5 tests per box)
December 3, 2021
WIZ Biotech COVID-19 / SARS-COV-2 Antigen Rapid Nasal Test, Approval Private Use / Self-administration by Lay Persons, CE1434, BfArM Listing (reimbursable), PEI evaluated (1 test per box)
December 7, 2021
Deepblue Medical Anhui COVID-19 / SARS-COV-2 Antigen Rapid Test LOLLY Layman's Test, Approval Private Use / Layman's Own Use, CE1434, BfArM Listing (Reimbursable) (1 Test per Box)
12,50 €
0,25 € / Piece
excl. tax plus shipping costs
Your selection: 100 pieces
Item number: deepblue_laientest_1er Categories: Lay tests / home tests, Lolly and saliva tests
According to the manufacturer, suitable for detecting the "Omikron", "Eris" and "Pirola" variants.
Deepblue Medical SARS-CoV-2 Antigen Lay Test Lolly Test (Pack of 1)
The COVID-19 Antigen Rapid Test Cassette is a lateral flow immunoassay method for the qualitative detection of SARS-CoV nucleocapsid antigens in swabs from individuals suspected of COVID-19 infection.
The results are used to identify the SARS-CoV-2 nucleocapsid antigen. This antigen is usually detectable during the acute phase of the infection. Positive results indicate the presence of viral antigens.
Details:
- Sensitivity: 96.40%
- Specificity: 99.80%
- Lay test - BfArM registered
- BfArM special approval for laypersons 5640-S-086/21
- BfArM Test ID: AT031/20
- Each test is individually packaged
- Lolly test
- Results already after 10 - 15 minutes
- Hygienic packing
- CE1434
- EU-RAT Listing No. 2651
Scope of delivery per unit:
- Test cassette
- Lolly
- Extraction reagent
- Tube with dropper cap
- Operating instructions
Notes on sales by PSA partners
Do you have any further questions about our range? Contact us and we will be happy to help you. Order the BfArM-registered rapid test and other high-quality protective equipment from PSA-Partner now.
Why PSA Partner?
- Certified PPE store
- Best ratings on the net
- Fair and transparent prices
- Payment on account
- No waiting times - only stock items
- Best references
Trusted Shops Reviews:
| Quantity | 50 |
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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 bottlenecks or endanger public safety, may also obtain and use rapid antigen tests for the detection of the SARS-CoV-2 coronavirus.
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.
Why PSA Partner?
- Certified PPE store
- Best ratings on the net
- Fair and transparent prices
- Payment on account
- No waiting times - only stock items
- Best references
Trusted Shops Reviews:
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