RADIMED GmbH works as a manufacturer of medical products based on the international standard DIN EN ISO 13485 in the areas of development, production and sales and is certified by a notified body as part of the conformity assessment of the respective medical products according to Annex V of the Directive 93/42/EEC.

All Radimed GmbH products meet the strict requirements of our internal quality guidelines and, of course, all the specifications required by the Medical Devices Directive 93/42/EEC and its national implementations.

If you have any questions about our quality management, Mr. Klein is at your disposal under the following contact details:

Tel.: 0234/ 89 00 290 or email: info@radimed.de

Our philosophy:

The increasing cost pressure in the healthcare sector is presenting medical technology companies with serious problems. As in other sectors, concentration and the associated synergy effects seem to be the panacea for reducing costs. However, it is often overlooked here that as the company grows, the important and intensive contact with the doctor as a customer and source of ideas is lost.

Our experience in the development and "approval" of medical devices and the efficient company structure enable us to offer cost-effective products and at the same time to implement customer developments (also niche solutions) quickly and ready for the market with the supporting consulting service from a single source.

The close contact to the customer and the prompt decision-making in a company of our size results in a significantly higher flexibility in the implementation of customer developments, for which the competition often no longer has resources. Speed in placing these developments on the market is another must, so that the fast AND competent reaction to customer inquiries is a key point of our strategy.

Radimed - Model M-Kath - Epidural Catheter

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