EU Market Access. Authorized.
Bringing your products safely to the EU Market
Services
European Representative for
- Medical devices according to MDR (EU) 2017/745
- In vitro diagnostic medical devices according to IVDR (EU) 2017/746
- Personal protective equipment according to PPE (EU) 2016/425
- Toys according to TSR (EU) 2025/2509
- Commercial and consumer products according to GPSR (EU) 2023/988
Consulting
As part of our mandate as European Authorised Representative, we are happy to advise you on Regulatory Affairs and Compliance upon request, so that you, as a manufacturer, can keep track of the specific requirements of the European market that may arise when placing your products on the market.
Registration
As part of our mandate as European Authorized Representative, we will gladly handle the necessary registrations for your products at European level (e.g. EUDAMED) as well as for the German market, upon your request.
About us
We, LUREMAH GmbH, are a young company founded in October 2025 in Germany by practitioners and specialists from the healthcare sector with many years of specific experience in both direct patient care and in the field of regulatory affairs and compliance.
Why us
Our goal is your products.
Our focus is on long term partnerships.
We are your active strategic partner.
Our company headquaters are centrally located in the European Union.
We have broad and in-depth expertise in the field of European product law.
We offer direct contacts, personal support and reliable communication.
You determine the scope of services according to your individual needs.
We are satisfied when they are satisfied.
Safety is our top priority.
Do you have any questions or would like a quote?
call us:
+49 151 7242324
write us: