Product compliance · CE / UKCA
EU & UK Authorised Representative (AR) services

Under Article 18 UCC and HMRC's representation rules, non-established businesses need an indirect customs representative to clear goods. flexfrontier takes on that role — and the joint liability that comes with it.

What is an Authorised Representative?

An Authorised Representative (AR) is an EU- or UK-established party appointed by a written mandate from a non-established manufacturer to carry out defined compliance tasks on its behalf. For CE marked products, Article 4 of Regulation (EU) 2019/1020 (the Market Surveillance Regulation) requires an economic operator established in the EU — a manufacturer, importer, Authorised Representative or fulfilment service provider — before most CE-regulated products can be placed on the market. For manufacturers selling direct without an EU importer, appointing an AR is the standard way to satisfy the rule.

The UK mirrors the model for the GB market: UKCA-marked products from overseas manufacturers need a UK-established party carrying the equivalent obligations — commonly called the UK Responsible Person or UK Authorised Representative depending on the product legislation. Since Brexit, one representative can no longer cover both markets: an EU AR does not count for the UK, and vice versa. flexfrontier provides both under one agreement.

16 Jul 2021

Since this date, Art. 4 of Reg. (EU) 2019/1020 bars CE-marked products from the EU market without an EU-established economic operator

20+ frameworks

CE marking spans the LVD, EMC, RED, Toys, Machinery, PPE, RoHS and more — the AR must know which apply to your product

10 years

How long the Declaration of Conformity and technical documentation must be kept at authorities' disposal

What the Authorised Representative actually does

  • Holds the technical documentation and Declaration of Conformity at the disposal of market surveillance authorities, typically for 10 years after the last product is placed on the market.
  • Appears on your product — the AR's name, registered trade name and address go on the product or its packaging and accompanying documents.
  • Verifies the compliance dossier — checking that the DoC exists, cites the right legislation and standards, and matches the product actually shipped.
  • Deals with market surveillance authorities — answering requests for information and documentation in the required language.
  • Cooperates on corrective action — supporting risk elimination, withdrawals and recalls, and informing authorities where a product presents a risk.
  • Registers products where required — sector databases and registrations that the legislation attaches to the AR role.

CE and UKCA markings, explained

CE marking is a legal declaration, not a quality stamp. By affixing it, the manufacturer declares — on its own legal responsibility — that the product meets every piece of EU harmonisation legislation that applies to it: the Low Voltage Directive for mains electronics, EMC for anything electrical, the Radio Equipment Directive for wireless products, the Toy Safety Directive, the PPE and Machinery frameworks, RoHS for hazardous substances, and more. No authority "issues" a CE mark: the manufacturer runs the conformity assessment, compiles the technical file, signs the Declaration of Conformity and applies the marking — involving a notified body only where the legislation demands third-party assessment (many toys, most PPE categories, some radio and machinery products).

UKCA is Great Britain's post-Brexit counterpart — same logic, UK legislation, UK-designated approved bodies. In practice the UK has announced indefinite recognition of CE marking for many product areas, including most consumer electronics, toys and machinery, so a compliant CE-marked product can generally continue to be sold in Great Britain. UKCA remains in use, certain sectors keep their own UK rules, and Northern Ireland follows EU rules under the Windsor Framework — so the right marking strategy depends on your product and channels, which we confirm during onboarding rather than leaving you to guess.

CE marking UKCA marking
Territory EU / EEA — and Northern Ireland Great Britain (England, Scotland, Wales)
What it declares Conformity with all applicable EU harmonisation legislation Conformity with the equivalent UK regulations
Third-party assessment EU notified body, where legislation requires it UK approved body, where legislation requires it
Accepted in the other market? CE recognised in Great Britain indefinitely for many product areas UKCA is not recognised in the EU
Representative needed by a non-established manufacturer EU-established economic operator (Art. 4) — typically an Authorised Representative UK-established representative for UKCA-scope goods
Marking rules Visible, legible and indelible; minimum 5 mm height with proportions maintained; on the product, or on packaging/documents where the legislation allows

Where your Authorised Representative appears on the product

Several CE frameworks and Article 4 require the economic operator's name, registered trade name and postal address on the product — or, where size makes that impossible, on the packaging or an accompanying document. Your AR's details sit alongside your manufacturer details, next to the markings themselves. We supply the exact wording for your rating plates and artwork, and review labels before you print.

  • On the product: manufacturer + AR name and address, model, batch or serial for traceability.
  • Markings: CE (and UKCA where used) at minimum 5 mm, proportions intact — plus WEEE bin and other framework-specific symbols.
  • In the paperwork: the AR named in the Declaration of Conformity and reachable in the language authorities require.
YOUR BRAND™ Smart Plug · Model SP-14 · 230 V~ 50 Hz
Manufacturer Your Brand Co., Ltd — Shenzhen, CN
Batch / Serial LOT 2026–A208
Standards EN IEC 60669 · EN 300 328 · EN 18031
EU Authorised Representative flexfrontier Ltd [EU office address] · info@flexfrontier.com
CE UK CA

Which products need an AR?

The Article 4 requirement covers most of the high-volume CE legislation: the Low Voltage Directive, EMC, RoHS, the Radio Equipment Directive, the Toy Safety legislation, machinery, PPE, gas appliances, pressure equipment and construction products, among others. In practice, if your product carries a CE mark and you have no EU importer taking on the obligations, you need an EU AR. The UKCA regime imposes the parallel requirement for goods sold into the United Kingdom.

Sector regimes add their own versions of the role: medical devices require an EU Authorised Representative under the MDR/IVDR and a UK Responsible Person registered with the MHRA; cosmetics require a named Responsible Person under the EU and UK Cosmetics Regulations. flexfrontier covers these regulated categories as part of the same engagement.

Your situation AR needed? Why
Non-EU manufacturer selling CE-marked products direct to the EU (D2C, Amazon, TikTok Shop) ✓ Yes No EU importer in the chain — Art. 4 requires an EU-established economic operator, and the AR is the practical answer
Electronics, smart home & wireless devices ✓ Yes LVD / EMC / RED all apply — RED now including cybersecurity requirements (EN 18031)
Toys and children's products ✓ Yes Toy Safety Directive — often with notified-body involvement and strict documentation
PPE, machinery, measuring instruments ✓ Yes Framework-specific AR duties; the Machinery Regulation tightens further from January 2027
Selling UKCA/CE-scope goods into Great Britain ✓ UK-side A separate UK-established representative is needed — we provide both under one agreement
Selling through an EU-established importer ✗ Not mandatory The importer can be the Art. 4 economic operator — though many brands still appoint an AR to keep control of the technical file
Non-CE consumer products (furniture, apparel, homeware) ✗ Different role They need a GPSR Responsible Person instead — one flexfrontier mandate can cover both
Medical devices ✗ Separate regime MDR/IVDR require an EC REP with EUDAMED registration — a distinct appointment we also provide
Cosmetics ✗ Separate regime The Cosmetics Regulation has its own Responsible Person with CPNP notification duties

AR vs GPSR Responsible Person vs importer — who does what?

These roles overlap on labels but sit under different laws, and many products need more than one:

Role Legal basis Covers
Authorised Representative CE/UKCA legislation + Reg. 2019/1020 Art. 4 Conformity documentation, technical file, market surveillance for CE/UKCA products.
GPSR Responsible Person Reg. (EU) 2023/988 Art. 16 General safety of virtually all consumer products — CE marked or not.
Importer Product legislation + customs law Takes on compliance obligations when it places goods on the market; can remove the need for an AR where one exists and accepts the role.

A consumer electronics product sold direct from outside the EU typically needs an EU AR (for EMC/LVD/RoHS) and a GPSR Responsible Person — a role our AR mandate is drafted to absorb, so one appointment covers both. See our GPSR Responsible Person service.

Marketplace reality: Amazon, and increasingly other platforms, require a valid EU Responsible Person / AR on file and on the listing for CE-regulated and consumer products — and suspend listings without one. An AR appointment is now a marketplace-access requirement, not just a legal formality.

Authorised Representative for Amazon, TikTok Shop and e-commerce brands

E-commerce is where AR gaps get found. Amazon retired its own Responsible Person programme, so sellers of CE-marked products — electronics, toys, PPE, radio equipment — must now provide their own EU economic operator details, on the listing and on the product. TikTok Shop and other platforms apply the same checks as they open EU marketplaces, and a listing without a valid EU operator is suppressed rather than fined. Selling on amazon.co.uk adds the UK layer: a separate UK-established representative for UKCA-scope goods.

We cover the full e-commerce stack under one agreement: EU AR and UK representation, labelling wording for products and packaging in the format platforms verify, compliance-document uploads during marketplace audits, and — because most consumer products also fall under the GPSR — the Responsible Person role folded into the same mandate. One appointment, every channel: Amazon EU and UK, TikTok Shop, your own store, and retail distribution.

How our AR service works

Step 01
Review & mandate

Because we share your liability, onboarding starts with a short compliance review of products and documents — most clients complete it within 24 hours.

STEP 02
We declare for you

Declarations filed in our name on your behalf through CDS and the EU national systems, with the correct representation codes — and CBAM authorisation where your goods need it.

Step 03
Duty & VAT settled

Charges handled at the border and passed through at cost, itemised — with import VAT flowing to your own registration so recovery stays in your hands.

Step 04
Records & defence

Every declaration archived audit-ready. If customs queries a declaration we signed, we stand behind it — that is what the shared liability means.

Authorised Representative pricing

AR services are priced as an annual fee per manufacturer, scaled by product range and risk category, with EU-only, UK-only and dual-market packages. Documentation review is included in onboarding, and there are no per-query charges when authorities contact us. Quotations are issued the same day.

FAQ
Authorised Representative — FAQs
  • What is an EU Authorised Representative?

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    An EU Authorised Representative is an EU-established party appointed by written mandate from a non-EU manufacturer to hold the technical documentation and Declaration of Conformity, appear on the product labelling, and deal with market surveillance authorities on the manufacturer's behalf under CE marking legislation and Article 4 of Regulation (EU) 2019/1020.

  • Do I need an Authorised Representative if I have no EU entity?

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    If your products are CE marked and you sell into the EU without an EU importer taking on the obligations, yes — Article 4 of the Market Surveillance Regulation requires an EU-established economic operator, and an AR is the standard way for a direct-selling manufacturer to comply.

  • Does an EU Authorised Representative cover the UK too?

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    No. Since Brexit the EU and GB are separate regimes: UKCA products sold in the United Kingdom need a UK-established representative, and CE products in the EU need an EU-established one. flexfrontier provides both under a single agreement.

  • Does the AR's name have to appear on my product?

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    Yes. Under Article 4 the name, registered trade name and postal address of the EU economic operator must appear on the product or on its packaging, parcel or accompanying document. We supply the exact wording and check your artwork during onboarding.

  • What is the difference between an Authorised Representative and a GPSR Responsible Person?

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    The AR operates under CE/UKCA conformity legislation and holds the technical file for those regimes; the GPSR Responsible Person is required under Regulation (EU) 2023/988 for virtually all consumer products, CE marked or not. Many products need both — our mandate is drafted so one appointment with us covers the two roles.

  • Can my EU distributor or importer act as my Authorised Representative?

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    An EU importer placing your goods on the market takes on its own obligations, which can satisfy Article 4 without an AR. But relying on distributors means their details go on your products, they see your technical file, and your market access depends on that commercial relationship — which is why most brands prefer an independent AR.

  • What happens if I sell CE products in the EU without an AR?

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    The product is non-compliant: customs can detain shipments, market surveillance can order withdrawal, and marketplaces suspend listings that lack a valid EU economic operator. Penalties are set by member states and can include fines and sales bans.

  • Do medical devices and cosmetics need something different?

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    Yes — sector regimes have their own representative roles: an MDR/IVDR Authorised Representative plus a UK Responsible Person registered with the MHRA for medical devices, and a named Responsible Person under the EU and UK Cosmetics Regulations. We provide these as part of the same engagement.

  • How quickly can an Authorised Representative be appointed?

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    The mandate can be signed within 24 hours. Documentation review and labelling updates follow immediately, so most manufacturers are compliant on the AR requirement within days rather than weeks.

  • What is CE marking and who applies it?

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    CE marking is the manufacturer's own legal declaration that a product conforms to every piece of EU harmonisation legislation applying to it. No authority issues it: the manufacturer performs the conformity assessment, compiles the technical file, signs the Declaration of Conformity and affixes the marking — using a notified body only where the specific legislation requires third-party assessment.

  • Is UKCA marking still required, or does the UK accept CE?

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    The UK has announced indefinite recognition of CE marking for many product areas, so compliant CE-marked goods can generally continue to be sold in Great Britain. UKCA remains valid and some sectors keep UK-specific rules, while Northern Ireland follows EU rules. What does not go away is the representation requirement — non-UK manufacturers still need a UK-established representative for the GB market, which we provide alongside the EU appointment.

  • Do we need a notified body?

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    Only where the applicable legislation demands third-party conformity assessment — common for many toys, most PPE categories, certain radio equipment and machinery moving into the new Regulation's high-risk categories. For most electronics under the LVD, EMC and standard RED routes, manufacturer self-assessment against harmonised standards is sufficient. We confirm the correct route per product during onboarding.

  • How must CE and UKCA markings be displayed?

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    Visibly, legibly and indelibly on the product, at a minimum height of 5 mm with the official proportions maintained — moving to the packaging or accompanying documents only where the legislation allows it for small products. Alongside the marking, the manufacturer's (and where applicable the economic operator's) name and postal address must appear. We check artwork against these rules before you print.

  • What is the difference between an Authorised Representative and a GPSR Responsible Person?

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    The AR is a framework role under CE legislation, appointed by written mandate to hold the technical file and deal with authorities for CE-marked products. The GPSR Responsible Person is the traceability role under Regulation 2023/988 covering virtually all consumer products. CE-marked consumer goods typically need both functions — our mandate is drafted so one flexfrontier appointment covers the two, in the EU and the UK.

    What happens if we sell CE-scope products without an economic operator?

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    The product cannot lawfully be placed on the EU market. In practice: marketplaces suppress listings that lack the economic-operator details, customs and market surveillance can detain or order withdrawal of goods, and national penalties apply. Because Article 4 details must also appear on the product or its accompanying documents, non-compliance is visible at a glance — it is the first thing an inspector checks.