We are your leading partner for development, manufacturing and registration of medical and industrial products in high-end applications. Whether prototypes or finished products in small- and large series: epmodex stands for highest precision, optimal solutions and a reliable partnership.
Hall 2 / F 2187
Hall 2 / F 2187
Since May 26th 2021, the Medical Device Regulation is fully applicable. Hence, all processes related to design, industrialization, manufacturing, marketing and market surveillance have to be aligned with the quality management system which must be compatible with ISO 13485:2016 and/or USA QSR.
epmodex AG, a medtech service provider from Duebendorf, developed, certified and produced a diagnostic system for the temporomandibular joint. The production of this high-precision system was carried out by our production partner Wymed AG.
On May 26, 2021, the Medical Device Ordinance came into force. All EU manufacturers therefore have to comply with specific Swiss requirements per MedDO and the appointment of a Swiss-AR for all medical devices imported into Switzerland. As your new Swiss-AR epmodex will support you.
After more then 10 years in the market, we develop and manufacture highly innovative medical device projects and are the leading partner to implement serial product quantities for market release. Our success is based on the fact that with our know-how we can bring new, innovative medical products more rapidly and successfully to the market.Today, short time-to-market times are particularly important since the market is very competitive and these projects are primarily capital driven. Whether a product receives approval one year sooner or later is critical! In this way we provide our customers with important strategic- and competitive advantages.
HauptsitzHochbordstrasse 98600 Dübendorf
Product Development and Consulting
Regulatory and Quality
Customer Service / Member of the Board
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