Oemeta metalworking fluids meet the high requirements of medical technology

The technological and regulatory requirements of the medical industry are exceptionally high, as the manufactured parts are intended to remain in the body for up to several years, depending on the application. A wide range of materials, some of which are new, are used for this purpose and their processing can be extremely complex. Oemeta offers exactly the right solutions for these requirements.

On the regulatory side, important aspects such as human compatibility, regulated ingredients with regard to the environment, biocompatibility and much more must be taken into account. Seamless documentation plays a key role in compliance implementation here. Oemeta is always available as an expert and partner for all topics relating to compliance implementation.

Auditing in medical technology is very extensive. Oemeta provides support here with customer-specific data documentation on all metal working fluid parameters that are necessary for compliance with the documentation obligation in accordance with ISO 13485 (Medical Devices Quality Management System). This also includes the data of the Oemeta product portfolio, which is qualified as "non-cytotoxic" according to DIN-EN 10993-5.

The product portfolio developed for medical technology includes oil-free and oil-based products as well as cleaners. This covers the entire process chain for metal, glass and ceramic machining. The cost-effectiveness of Oemeta metalworking fluids is guaranteed by reduced tool and operating costs or reduced downtimes. The focus is on continuous and holistic process optimization and stabilization.