We would like to point out to EXPLIXIT that the PPE products purchased by DCHT GmbH are NOT medical devices and are only intended for self-protection. The products are subject to the PPE 2016/425 regulation.
COVID 19 Ag rapid tests may only be used by medically trained personnel.
COVID 19 ANTERIO NASAL tests are for self-testing according to §323c/Abs. 18 BAO suitable.
COVID 19 Ag lay test are approved by special approvals according to §11 paragraph 1 Medical Devices Act (MPG) of antigen tests for self-administration by lay persons (self-tests) for the detection of SARS-CoV-2
DCHT GmbH does not assume any liability for damages caused, such as leaked buffer solutions, elements missing from the packaging by the manufacturer. DCHT GmbH also assumes no liability for improper use or incorrect results of the tests.
With the acceptance of an offer of DCHT GmbH the above mentioned clarification is accepted.
Orders cannot be cancelled or returned.
The Management Board, January 2021