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Even the strongest men need a little help sometimes…as the staggering demand for large and heavy OP-Film rolls is rapidly increasing.

Our new weight lifting tool is just another trick to keep up with the many inquiries (and to spare the back of our machine operators!)

The week of November 13-17 has definitely been the most intense week of the year 2023 for our team. After four full days at the tradeshow MEDICA healthcare in Dusseldorf, Germany, we gathered our guests for what turned out to be an amazing customer event. The best of two worlds. Indispensable counterparts: Eurotape and Somed.

The exciting full day program on Friday 17 was filled with informative seminars by external speakers, interactive workshops by our lab team, and an exclusive tour of our production plant. It is available to download to have a flashback of what we call the highlight of our corporate year.

It has been the perfect occasion to learn more about reusable and single use draping systems for operating theaters. In our industry it is about connecting with care and we have one common goal: to deliver high quality healthcare.

We are proud of our international network and dedicated employees. At Soest Medical Group the best of the world was represented respectfully and peacefully in many ways.

Enjoy the pictures and don’t forget to sign up for the next occasion!

Every hospital management who is supportive of a sustainable strategy should at least consider using reusable high technical surgical textiles in their operating theaters. This video illustrates how Eurotape wash soluble products are applied on reusable textiles and processed in the clean room of an industrial laundry.

We are pleased to announce that as of today, 1 September 2021, SMG adds the Duplomed drape tapes from Lohmann to their Eurotape portfolio.

We invite you to read the joint statement of the CEO’s of both SMG and Lohmann.

We are pleased to announce that EUROTAPE b.v. entirely works under the regulations (EU) 2017/745 regarding the Medical Device Regulations. The MDR, or Medical Device Regulations, refers to a set of regulations implemented by the European Union (EU) to establish a comprehensive framework for the regulation of medical devices. The MDR replaced the previous Medical Device Directive (MDD) and came into effect on May 26, 2021.

The primary goal of the MDR is to ensure the safety, quality, and efficacy of medical devices while enhancing patient safety and harmonizing regulations across EU member states. The regulations apply to a wide range of medical devices, including surgical instruments, implants, diagnostic equipment, software, and more. The MDR represents a significant shift in the regulation of medical devices, with an increased focus on patient safety, transparency, and accountability. Compliance with the MDR is mandatory for all medical device manufacturers wishing to market their products within the European Union.

Any questions regarding the MDR, feel free to contact us here!