No because not all Greiner Bio-One products are medicine products or In-Vitro Diagnostics. For all CE products there are CE Declarations of Conformity which do not have to be confirmed by a notary.
Only medicine products or In-Vitro Diagnostics of a higher risk class are controlled with notofied body (e.g. TÜV). In this case there exists a Control Certificate. This only applies for the Greiner Bio-One products Swab Tubes and Swabs....
The manufacturer can concerning abusiveness of the CE Marking, e.g. to get some advantages in the competition, getting indicated. In this case he has to put the product out of the market and he also makes himself indictable.
The reason is that not all Greiner Bio-One products are medicine products or In Vitro Diagnostics, but some are general laboratory products too.
All products which are listed according definition in the EU Directive have to be marked with CE, e.g. all products which are considered as medicine products according their definition.
If a product is defined under EU Directive some guidelines have to be observed. The observation of these requirements regarding the manufacturing and product safety according the EU Directive e.g. for medicine products or In Vitro...
