Find­ing your EU Autho­rized Rep­re­sen­ta­tive* is like find­ing the love of your life. Pity is, you already might have found the right one, but you just can’t believe your luck. So we are hap­py to give you six rea­sons for get­ting seri­ous with mdi Europa.

Six rea­sons why you have found the right one

1. We don’t waste your time and money

As a small team of high­ly ded­i­cat­ed experts we oper­ate effi­cient, flex­i­ble and economical.

2. We care about size

We spe­cial­ize in small and medi­um-sized enter­pris­es, that’s why we exact­ly know their chal­lenges and needs.

3. Hon­esty is self-evident

We don’t defraud you with hid­den costs.

4. We have proven our strength

Since 2000 our team reg­is­tered hun­dreds of med­ical device man­u­fac­tur­ers for CE Mark­ing with the Euro­pean com­pe­tent authorities.

5. You are family

Because we are a fam­i­ly owned busi­ness, we know all about trust and reli­a­bil­i­ty and you will be treat­ed like you’re one of us.

6. We will intro­duce you to our friends

You can prof­it from our net­work of experts with excel­lent reg­u­la­to­ry ser­vices around the world.

Are you convinced?

Well, that’s won­der­ful! If you have fur­ther ques­tions or want direct­ly offer us the part­ner­ship, you are very wel­come to get in touch with our team.

Still not convinced? 

You are right! Choos­ing your Euro­pean Autho­rized Rep­re­sen­ta­tive shouldn’t be done in a rush. So you are wel­come to study some infor­ma­tive arti­cles and pages on Fol­low­ing we have assem­bled use­ful links for your inquiries. 

You already have announced an EU Autho­rized Representative

But you are not hap­py with the rela­tion­ship? No prob­lem! You should read our arti­cle “How to change your EU Autho­rized Rep­re­sen­ta­tive”.

* As defined in the Med­ical Devices Reg­u­la­tion (EU) 2017/745 (MDR), the In Vit­ro Diag­nos­tic Med­ical Devices Reg­u­la­tion (EU) 2017/746 (IVDR), the Active Implantable Med­ical Devices Direc­tive 90/385/EEC (AIMDD), the Med­ical Devices Direc­tive 93/42/EEC (MDD) and the In Vit­ro-Diag­nos­tic Med­ical Devices Direc­tive 98/79/EC (IVDD).