News

Visit from the Danish Medicines Agency

Wolturnus has had a visit from the Danish Medicines Agency to review our systems and practices for compliance with the new Medical Device Regulation (MDR). And we’re happy to inform...

Christmas time 🎄🎅

Merry Christmas and a Happy New Year! Christmas is just around the corner, and we would like to thank our customers and partners for an exciting 2022. We look forward...

Wolturnus works with Sustainable Development Goals

         How Wolturnus work with 6 selected Sustainable Development Goals At Wolturnus, we pay special attention to the United Nation’s Sustainable Development Goals and are working with selected...

Ascension Day, 26 & 27 May

Due to the upcoming Ascension Day, the Wolturnus office and production will be closed on May 26 & 27. Photo Credit: www.th-10.de

Merry Christmas and a Happy New Year

Christmas is once again knocking on the door. We would like to thank all our customers and partners for a good yet challenging year. During the holiday period we will...

New in the team: Marco Hessler  

We are happy to welcome Marco Hessler as new Portfolio Manager for our further growth in the team. Marco will enrich our team in Denmark and Germany with his wide...

New sponsorship with Edina Müller

Paracanoeing athlete Edina Müller  We are excited to inform you about the cooperation with Germany’s most successful paracanoeing athlete: Edina Müller. The Wolturnus GmbH supports Edina as a wheelchair mobility...

Jetze Plat – Tokyo 2020

The Paralympic Games The countdown for the Paralympic Games in Tokyo has begun. We are excited to follow our Wolturnus athlete Jetze Plat who is participating at his third Paralympic...

Happy summer!

From July 19 to August 6 our production department has reduced workforce but is still handling urgent cases. Our customer service has normal opening hours all summer. We wish all...

New Medical Device Regulation (MDR) comes into application

Today, the new Medical Device Regulation (MDR) replaces the former Medical Device Directive (MDD). MDR is a new set of regulations that we as a Class 1 medical device manufacturer...