★★★★★
Trusted by +120 global manufacturers & brands

Market access · 🇫🇷 France

Product certification for France

EU CE rules + French language and DGCCRF enforcement

France follows EU CE legislation with strong emphasis on French-language instructions, consumer information, and DGCCRF / customs enforcement.

France is an EU Member State. Core product law is EU-wide (CE marking). This page adds local authorities, language, and market-surveillance practice on top of the EU framework.

Full EU deep-dive

How France regulates products

Place products on the French market only with full EU conformity (CE, DoC, technical file). French Consumer Code and language rules require French safety information for consumers. Market surveillance involves DGCCRF and specialized agencies depending on product type (radio, medical, etc.).

Key frameworks

  • CE marking (EU Single Market)
  • LVD / EMC / RED as applicable
  • RoHS & REACH
  • National language labeling & market surveillance

Regulatory bodies

Who sets the rules, who certifies, and who enforces — by role.

European Commission / NANDO Notified Bodies

EU product legislation framework; lists Notified Bodies by directive

DGCCRF

Consumer product market surveillance

ANFR

Radio spectrum / radio equipment checks

Customs (DGDDI)

Import controls

INERIS / Notified Bodies (Ex context)

ATEX / industrial interfaces when relevant

Safety, EMC, wireless, FuSa & more

For each domain: authority, regulations, typical standards, reports, and marking.

Electrical safety

Manufacturer self-declaration; market surveillance by Member State authorities; Notified Bodies when required by other legislation

Regulations

  • Low Voltage Directive 2014/35/EU (LVD)
  • General Product Safety Regulation (EU) 2023/988 (GPSR) where consumer products apply

Standards

  • EN IEC 62368-1 (AV/IT)
  • EN 60335 series (household)
  • EN 61010-1 (lab/measurement)
  • EN 60598 (luminaires)

Reports / evidence

  • Safety test report to harmonized EN
  • Risk assessment / construction review
  • EU Declaration of Conformity

Marking

CE mark on product / packaging / instructions as applicable

LVD is typically Module A (internal production control) — no mandatory Notified Body for most products.

EMC

Manufacturer; optional EMC Notified Body; national market surveillance

Regulations

  • EMC Directive 2014/30/EU

Standards

  • EN 55032 / EN 55035 (multimedia)
  • EN IEC 61000-6-x (generic)
  • EN 61326 (industrial/lab)
  • EN 50121 (rail) when applicable

Reports / evidence

  • EMC emissions & immunity test reports
  • EMC assessment / technical construction file if used

Marking

CE (EMC is part of overall CE claim)

Wireless / radio

Manufacturer; Notified Body for certain radio modules / unavailable harmonized standards; national spectrum authorities for use conditions

Regulations

  • Radio Equipment Directive 2014/53/EU (RED)
  • Delegated cyber acts under RED Art. 3(3) where in force for product classes

Standards

  • EN 300 328 (2.4 GHz)
  • EN 301 893 (5 GHz)
  • EN 301 489 series (EMC for radio)
  • EN 62311 / EN 50385 (RF exposure)
  • EN 18031 series (cyber, where mandated)

Reports / evidence

  • RF test reports
  • RED DoC
  • Notified Body EU-type examination certificate when Module B applies

Marking

CE; Notified Body number on label if Module B/C used

Intentional radiators are assessed under RED (not separately under LVD+EMC for radio aspects).

Machinery & robotics

Manufacturer; Notified Body for Annex I / high-risk categories

Regulations

  • Machinery Directive 2006/42/EC (current)
  • Machinery Regulation (EU) 2023/1230 (applies from 20 Jan 2027)

Standards

  • EN ISO 12100
  • EN ISO 13849-1
  • EN IEC 62061
  • EN ISO 10218 / ISO/TS 15066 (robots/cobots)

Reports / evidence

  • Risk assessment
  • Technical file
  • EU DoC or Declaration of Incorporation (partly completed machinery)

Marking

CE on complete machinery; partly completed machinery uses DoI, not CE

Functional safety (FuSa)

No single EU “FuSa mark”; evidence via Machinery / sector directives and customer SIL/PL requirements; Notified Bodies for certain safety components

Regulations

  • Machinery Directive / Regulation essential requirements
  • Sector rules (rail, process, medical) as applicable

Standards

  • IEC 61508
  • ISO 13849
  • IEC 62061
  • IEC 61511 (process)

Reports / evidence

  • FMEA / FMEDA
  • SIL/PL assessment reports
  • Safety manual / safety case excerpts

Marking

Usually no standalone FuSa mark — claimed via DoC + safety documentation

Explosive atmospheres (ATEX)

Notified Bodies for Category 1 / M1 and many Category 2 paths; manufacturer + NB for production QA (QAN)

Regulations

  • ATEX Directive 2014/34/EU
  • ATEX workplace Directive 1999/92/EC (user side)

Standards

  • EN IEC 60079 series
  • EN ISO 80079-36/-37 (non-electrical)

Reports / evidence

  • EU-type examination certificate
  • QAN / quality assurance notification
  • Ignition hazard assessment

Marking

CE + Ex hexagon + equipment group/category + EPL marking

Materials / substances

ECHA (REACH); national enforcement for RoHS / packaging

Regulations

  • RoHS Directive 2011/65/EU (as amended)
  • REACH Regulation (EC) 1907/2006
  • POPs, SCIP database obligations

Standards

  • EN IEC 63000 (technical documentation for RoHS)
  • IEC 62321 series (test methods)

Reports / evidence

  • Material declarations / IPC-1752
  • Test reports for restricted substances
  • SCIP notification where required

Marking

CE claim includes RoHS where in scope; no separate RoHS logo required

Batteries & energy

Manufacturer; Notified Bodies for certain Battery Regulation conformity modules

Regulations

  • Battery Regulation (EU) 2023/1542
  • UN 38.3 (transport — often paired)

Standards

  • EN IEC 62133
  • EN IEC 62619
  • relevant EN for chargers / ESS

Reports / evidence

  • Battery conformity assessment evidence
  • UN 38.3 test summary
  • carbon footprint / due diligence where phased in

Marking

CE; battery labeling / passport requirements per timeline

French market practice

DGCCRF / ANFR

Regulations

  • EU acts
  • French Consumer Code language obligations

Standards

  • EN harmonized standards

Reports / evidence

  • EU DoC
  • French instructions for use
  • traceability of importer

Marking

CE; French warnings where required

Documents & reports typically needed

  • EU Declaration of Conformity (all applicable legislation listed)
  • Technical documentation (design, BOM, risk assessment, test reports)
  • Instructions for use in official language(s) of destination Member State
  • Authorized Representative mandate if manufacturer is outside the EU/EEA
  • Traceability / economic operator contact on product or packaging (GPSR / New Legislative Framework)

Marking summary

CE mark is mandatory for in-scope products placed on the EU market. Member-state language and national market-surveillance practices apply on top of EU law — not instead of it.

Typical pathway

  1. 1

    Confirm EU scope

    Identify every applicable directive/regulation — products often need several.

  2. 2

    Select standards

    Use current Official Journal harmonized (or common) standards for presumption of conformity.

  3. 3

    Test & assess

    Coordinate accredited labs; involve a Notified Body only when the legislation requires it.

  4. 4

    Document & mark

    Build technical file, sign EU DoC, affix CE, appoint EU AR if needed, localize labels/IFU.

Common pitfalls

Issues that delay customs, retail acceptance, or lab projects.

Missing French IFU / labels on consumer goods
Importer identity not available to MSAs
Radio products without RED evidence when ANFR checks

FAQ

Is there a France-only safety mark like GS?

CE is the legal mark. Sector marks exist, but France does not use GS; focus on CE + French documentation.

Planning France market entry?

We map regulations, build the test matrix, coordinate labs, and prepare marking and declarations — including multi-market stacks with EU, US, and beyond.

Book Free Consultation