European Union · Electronics

CE Marking for Electronics in the European Union

A practical guide to CE Marking for Electronics for electronics sold in the European Union: who it applies to, what to prepare, and the mistakes that cause rejection.

Who needs it

Electrical and electronic products placed on the EU market; Radio equipment and connected devices

Authority

EU market surveillance authorities

Legal basis

LVD 2014/35/EU, EMC 2014/30/EU, RED 2014/53/EU, RoHS 2011/65/EU

Local representative

Yes — an EU responsible person or importer is required

Timeline

Before placing the product on the EU market

Cost

Testing and certification fees vary by product and scope

If you do not comply

Withdrawal, recall, fines, and market surveillance action

Who needs this

Electrical and electronic products placed on the EU market
Radio equipment and connected devices

Documents you need

Technical file
Test reports for the applicable directives
EU declaration of conformity

Compliance checklist

Tick each item as you collect it. Saved in this browser only.

Technical file
Test reports for the applicable directives
EU declaration of conformity

How to comply

Identify which directives apply
Test against the applicable standards
Prepare the technical file and declaration
Apply the CE mark and importer details

Brief for your lab or agent

Copy this into an email, then edit the product and channel.

Request: CE Marking for Electronics — European Union
Product category: Electronics
Authority: EU market surveillance authorities
Legal basis: LVD 2014/35/EU, EMC 2014/30/EU, RED 2014/53/EU, RoHS 2011/65/EU

Documents we already have:
  1. Technical file
  2. Test reports for the applicable directives
  3. EU declaration of conformity

Questions:
  1. Does our product fall under CE Marking for Electronics in the European Union?
  2. Which test standards or evidence do you accept?
  3. What is the current fee and lead time?
  4. Is a local representative required, and can you act as one?

Cost and timeline

Before placing the product on the EU market.

Testing and certification fees vary by product and scope.

Common rejection reasons

Wrong directive scope identified
Declaration of conformity missing or incomplete
No EU importer or responsible person details

Registration, notification, or certification is not the same as approval. Keep the technical file current and make sure the label, listing, and submitted data match.