pheneo

For many years, there have been increasing requirements in medical technology with regard to cost efficiency and facilitating application.

Different levels of training, regulatory guidelines and laws in global markets also present you, a material OEM, with constantly new, intensive challenges.

We at pheneo have focussed on this stress area for a number of years. Not only with our own products, which meet current and future requirements, but also with customer-specific, exclusive developments, which we would be pleased to manufacture for you in a suitable production environment.

Development & Production of Application & Packaging Systems:

Unit Dose
Multi Dose
Technical Product Safety
Application Systems

Made in Germany

Quality, durability, reliability, efficiency, control, integrity, communication. These are the characteristics, which “Made in Germany” stands for in the world.

Our location is a clear commitment to these qualities.

Unlike many companies in our industry development, toolmaking and production are not located in low-wage countries, but now and in the future in Germany.

As a company, we want to set an example with this decision and assume social responsibility in our country.
This is because health products and consequently your health should be in the hands of professionals with an equally professional development environment. With this decision we are continually investing in specialised domestic production facilities and methods.

The result is an increase in both the flexibility and capacity of development and production. We therefore not only develop based on the capacity of our production facilities, but also according to your wishes. These are factors that ensure we enjoy new competitive advantages. Specialised, highly demanding markets require a high level of communication and a high degree of commitment and knowledge from our employees. This is how we ensure our long-term mutual business relationship and your market success.

ISO 13485 certified

Quality is one of the most important characteristics with medical products, because every defect can affect the efficacy of the product and the safety of the patient and user.

When registering a medical product or pharmaceutical product, creation of complete documentation is mandatory for you as OEM.
pheneo is therefore not only DIN EN 13485 certified and DIMDI (German Institute for Medical Documentation and Information) listed, but as part of our customer relations you also receive product-related, complete documentation and support for your documents to be submitted, both of which are internationally recognised.

And this not only applies to our own product range, but of course also for every exclusively developed product.
You thus avoid costs in monitoring the supply chain and shorten the internal process for creating the necessary documents.