
The EU Packaging and Packaging Waste Regulation (PPWR) presents companies with far-reaching requirements.
Sutter Medizintechnik is already proactively addressing the PPWR requirements and is laying the foundation for transparent documentation for customers, regulatory authorities, and business partners.
On 19 December 2024, the European Parliament and the Council of the European Union adopted the new Packaging and Packaging Waste Regulation (PPWR) as part of the European Green Deal. Following its publication in the Official Journal of the European Union on 22 January 2025, the Regulation entered into force on 11 February 2025. Most of its requirements will apply from 12 August 2026, unless specific transitional periods have been provided.
The objective of the PPWR is to significantly reduce packaging waste across the European Union, improve the recyclability of packaging, and strengthen the circular economy in a sustainable manner. In addition, the Regulation introduces binding requirements regarding the use of recycled content, the reusability and compostability of packaging, as well as packaging labelling.
Sutter Medizintechnik is continuously committed to designing packaging solutions that are compliant, resource-efficient, and future-ready. The requirements of the new European Packaging Regulation – Regulation (EU) 2025/40 (Packaging and Packaging Waste Regulation – PPWR) – are being progressively integrated into our packaging and labelling processes.
As a manufacturer of medical devices, product protection, sterility, patient safety, and regulatory compliance are key considerations in the development of our packaging solutions. At the same time, we are committed to optimizing material use, improving recyclability, and proactively addressing future PPWR requirements at an early stage.
Further Requirements for Recyclability, Material Efficiency and the Circular Economy
We continuously review our packaging solutions with regard to material selection, recyclability, and future regulatory requirements. The PPWR establishes harmonized, legally binding requirements across the European Union to support these objectives.
Where technically and regulatorily feasible, we work to optimize packaging volume and material usage without compromising the safety, performance, or integrity of our products. The PPWR will require packaging weight and volume to be minimized in the future.
Future packaging labels and digital information offerings will be further developed in line with regulatory requirements. The PPWR introduces harmonized labelling requirements and, in certain cases, digital information solutions, for example through QR codes.
Sutter continuously monitors and evaluates new requirements relating to recycled materials, reuse systems, and further developments within the European circular economy. Through this proactive approach, we aim to address future regulatory requirements at an early stage and contribute to a more sustainable use of resources.

Registered in the LUCID system and aligned with European and national requirements
The Sutter Medizintechnik GmbH fulfills its extended producer responsibility for packaging in accordance with applicable European and national regulations, in particular the Packaging and Packaging Waste Regulation (PPWR) and the German Packaging Act.
The company is registered in the LUCID packaging register of the Central Packaging Register Foundation under registration number DE5416960430206. The registration and associated master data are regularly reviewed and updated.
Participation in the registration system ensures that all relevant obligations regarding the collection, reporting, and recycling of packaging are fully met.
The Packaging and Packaging Waste Regulation (PPWR) is the European Union’s new framework for packaging and packaging waste. Its aim is to reduce packaging waste, enhance recyclability, and support the transition to a circular economy across Europe.
Yes. The PPWR generally applies to packaging used in many industries. However, specific rules and exemptions may apply to certain types of medical device packaging.
Disposal and recycling information will be provided through packaging labels and digital information solutions in the future.
Packaging solutions are continuously evaluated and improved. Any modifications are made with due consideration for product protection, regulatory requirements, and sustainability objectives.
Note: The information presented reflects our current understanding of the PPWR. Future regulatory changes and further clarifications of the Regulation remain subject to change.
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