EUREP

Your Authorized Representative in the EU

If you manufacture outside the EU, most CE-marked products need an economic operator established in the EU before they can be sold there. We take this role as your Authorized Representative by written mandate, with our name and address on your products.

Handshake over a tablet, scales in the background

You make CE-marked products outside the EU

You want to sell in the EU directly to customers, through distributors or on marketplaces. Buyers, platforms and authorities ask who your economic operator in the EU is, and your labels need a name and address there.

What applies to your products

Article 4 of Regulation (EU) 2019/1020 sets the basic rule for most CE-marked products.

  • An EU operator for CE products

    Products under the acts in Article 4(5), such as electrical and radio equipment, machinery, toys and PPE, need an economic operator established in the EU.

  • Four types of economic operator

    The role can be an EU manufacturer, your EU importer, an Authorized Representative with a written mandate or, as a fallback, a fulfillment service provider.

  • Name and address on the product

    The operator's name and postal address go on the product, its packaging, the parcel or an accompanying document.

  • Product design stays with you

    Design, manufacture and the technical documentation remain your tasks as manufacturer. As a rule, they cannot be delegated to a representative.

    Product Compliance & Documentation

What we do within the agreed scope

We act under a written mandate for the tasks it names, while responsibility for your product, its design, conformity assessment and Declaration of Conformity stays with you.

Talk to our team
  • Your Authorized Representative in the EU

    Appointed by written mandate within 24 to 48 hours once your product details and documents are complete.

  • Economic Operator support

    For each product and sales channel, we clarify who acts as your EU economic operator: your importer, a fulfillment provider or us.

  • Our details for your labels

    Our name and address for your product, packaging or accompanying document and, where your act provides for it, your Declaration of Conformity.

  • Documents ready for 10 years

    We keep your Declaration of Conformity and technical documentation available to market surveillance authorities for 10 years.

  • Contact for authorities

    We answer authority requests, provide your documents and cooperate on corrective action, always in close contact with you.

  • Annual review of your file

    Once a year we review your Declaration of Conformity and technical file and tell you what needs updating.

What we need from you

  • Product list with models and photos
  • EU Declaration of Conformity or a draft
  • Technical documentation and test reports
  • Labels, packaging artwork and user instructions
  • Company details and a named contact

How it works

  1. 01

    First conversation

    You tell us about your products, markets and sales channels. We name the rules and the EU role you need.

  2. 02

    Documents and mandate

    You send your documents. We review them, and you sign the written mandate that defines our tasks.

  3. 03

    Appointment

    Once your documents are complete, we confirm the appointment within 24 to 48 hours and send our details for labels.

  4. 04

    Ongoing support

    We answer authority requests, keep your documents available and review your file every year.

Not sure what your product needs?

Stefan HülsiggensenFounder and Managing Director

Talk to our team

Questions about the Authorized Representative

Do I need an Authorized Representative if I have an EU importer?

Not necessarily. Your EU importer can be the economic operator required by Article 4 of Regulation (EU) 2019/1020 for the products it places on the market. A representative helps where you ship directly to customers, sell through several importers or want one contact for authorities.

Which products need an EU economic operator?

Products under the acts listed in Article 4(5) of Regulation (EU) 2019/1020, including electrical equipment, EMC, radio equipment, RoHS, machinery, toys, PPE, gas appliances, pressure equipment, construction products and batteries. Most consumer products without CE marking need one under Article 16 of the GPSR.

Can the Authorized Representative sign the Declaration of Conformity?

Only if the applicable act allows it and the written mandate names this task. The declaration is still issued under the manufacturer's sole responsibility, and drawing up the technical documentation stays with the manufacturer unless the act provides otherwise (Blue Guide, section 3.2).

How fast can Representa become my Authorized Representative?

Usually within 24 to 48 hours once we have your product details and complete documents.

Does my EU Authorized Representative also cover Northern Ireland?

It can. Under the Windsor Framework, EU product rules apply in Northern Ireland, and operators that must be established in the EU may also be established there (Blue Guide, section 2.9.6). A company established only in Great Britain cannot take the role.

Insights on this topic

Tell us about your products

We look at your products and sales channels and tell you which EU role you need and which documents we need from you.

Get in touch with our team of experts

Tell us what you manufacture and where you want to sell. We identify the requirements for EU and UK market access and come back to you with the next steps.

Target market *

* Required