Industry position on the conformity assessment procedure for products in contact with drinking water

The EU Drinking Water Directive (Directive (EU) 2020/2184), which entered into force in January 2021, introduces for the first time EU-wide harmonized minimum hygiene requirements for materials and products in contact with drinking water. For the specific requirements, the EU Commission has to publish several legal acts with supplementary regulations by January 2024.


Industry position on conformity assessment

One of these legal acts will regulate the future conformity assessment procedure for products in contact with drinking water. A draft of this legal act is not yet publicly available. However, the industry initiative European Drinking Water, initiated by figawa, has already published a position paper with an explanatory scheme at this stage, after an intensive and lengthy coordination process, and submitted it to the EU Commission.

Based on experiences already made at national level, a pragmatic process is described, which is supported as a compromise by the entire value chain involved. The position paper focuses on plastics and other organic materials, proposing regulations that are proportionate to the potential impact on drinking water quality, particularly for products with a smaller surface in contact with drinking water such as sanitary taps.


UBA study supports industry position

At the same time as the position paper was published, the German Environment Agency released the final report of a study on the migration of substances from injection-molded components in contact with drinking water produced by different companies. The study was initiated by figawa and significantly supported by its member companies.

The results fully support the regulations described in the position paper. For example, the study concludes that the testing and evaluation of specifically manufactured test panels, and thus the certification of preliminary products (granules), appears to be a suitable way to reduce the testing effort for components manufactured at different locations.

A prerequisite for this, however, would be that the process parameters of injection molding are monitored and taken into account in the certification of the components. For certain components or products, a certificate for the preliminary product (granules) could thus be sufficient to demonstrate hygienic suitability with regard to the release of substances into drinking water.

Lars Neveling