UKCAThe CE mark for Great Britain

The new UKCA mark has been in force in the UK since 1 January 2021:

  • The UKCA marking (UK Conformity Assisted marking) is the UK marking for products placed on the market in the UK (England, Scotland and Wales) and replaces the EU requirements for CE marking.
  • Since the UK's membership of the EU came to an end on 31 January 2020 ("Brexit"), the UK has been in a transition phase in which it remains part of the EU single market.
  • This transition phase has been adjusted several times (the last time was 31 December 2024) and has now been suspended indefinitely.
  • For manufacturers, this means that products can still only be sold with the CE mark in the UK. Nevertheless, there are many manufacturers who value the UKCA mark.

The experts at easyCE will be happy to help you place your products on the market and assess special cases. We are happy to support you with CE, UKCA and other labelling.


You simply apply the CE mark and sign the Declaration of Conformity, worry-free
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Willy Lebherz

Director & founder of easyCE GmbH

Office background

Declaration of conformity done!

Receive your UKCA declaration of conformity ready for signature.

Risk assessment completed!

UKCA mandatory risk analysis conducted.

Relevant directives & standards applied!

Your product evaluated against relevant directives and standards.

Technical documentation created!

Receive a pragmatic, user-friendly operating manual.

UKCA mark attached!

Simply affix the UKCA mark and you're done.

Verstehen Sie die Besonderheiten Ihrer Branche bei der UKCA-Kennzeichnung

FAQ

What does the UKCA mark mean?

The UK Conformity Assessment Mark will, after a currently indefinitely suspended period, be a mandatory mark on products indicating conformity with UK legislation.

Will the CE marking remain valid for products placed on the UK market?

For most products placed on the UK market, the CE marking was only supposed to be valid until 31 December 2024 after multiple extensions. However, this deadline has now been suspended indefinitely. It is not yet possible to estimate when the UKCA mark will finally become mandatory.

What are the differences between the UKCA mark and the CE mark?

Many of the differences between the two systems are administrative in nature and reflect the fact that the UKCA only applies in the UK and only requires information in English.

What aspects of UKCA do not change compared to CE?

Many aspects are the same; the scope of products covered, the technical requirements (essential requirements, standards) and the conformity assessment procedures will all initially be the same.

How will the UKCA mark affect Northern Ireland?

Products placed on the market in Northern Ireland (and the EU) must be CE marked regardless of their origin. Products placed on the market in Great Britain must be UKCA marked as described above,

Can I apply both the CE and UKCA marks on my product?

Yes, provided they fulfil the associated requirements. It is already common practice to affix several conformity marks to products sold internationally.

What specific UK laws must be observed when marking UKCA?

To implement the new regulation, the UK government has issued several regulations (Statutory Instruments) to amend the current legislation. The most important regulations are the Product Safety

According to which standards must the UKCA marking be carried out?

The British Standards Institution (BSI) remains firmly committed to the EN and international standards systems and 'harmonised standards' remain best practice for both CE and UKCA marking.

What other measures are required for the UKCA marking?

Other aspects that have a direct impact on manufacturers and importers are

What is the impact of Regulations (EU)2019/1020 on UKCA labelling?

Regardless of the UK's exit from the EU, in July 2021, Regulation (EU)2019/1020 will introduce important changes to manufacturers' obligations that are likely to impact UK and other non-EU manufacturers wishing

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Approach to UKCA marking

Type and manner of support

Scope of support

Contact during project processing

Find the easiest way to obtain the UKCA mark

Abbreviated process for UKCA derived directly from CE

All-inclusive or modular – whatever you prefer

Personal contact with experts who take your wishes into account

other UKCA service providers

Often lacking in sound judgement and unnecessarily complicated

Mostly flexible but often bureaucratic

Mostly flexible in terms of support scope

Mostly personal contact

CE Software

Follows standardised process; special circumstances not taken into account

Double burden for you: software management + no support during processing

Only according to software scope and purchased modules

No contact

You want support that lightens your workload and doesn't create more work.

Reference Projects

CE marking of laboratory machines developed in-house

CE marking of laboratory machines developed in-house

In the course of an upcoming ISO 45001 occupational health and safety audit, easyCE supported a laboratory technology manufacturer in ensuring CE conformity for its internally used validation machines for medical equipment. Our specialists conducted a comprehensive assessment of occupational health and safety aspects and integrated these into the CE documentation. Particular attention was paid to safe operation by laboratory staff and the documentation of risk assessments that meet both CE and ISO 45001 requirements.

Takes into account, among others: 2006/42/EU, 2014/35/EU, 2014/30/EU, 2011/65/EU EN ISO 12100, EN 60204-1

CE marking for a laboratory robot

CE marking for a laboratory robot

In the course of an upcoming ISO 45001 occupational health and safety audit, easyCE supported a medical technology manufacturer in achieving CE conformity for its coagulation robot—a specialized laboratory machine for the automated performance of coagulation cycles for testing purposes. Our specialists conducted a comprehensive assessment of occupational health and safety aspects and integrated these into the CE documentation. Particular attention was paid to the safe handling of electrosurgical components and the documentation of risk assessments that meet both CE and ISO 45001 requirements.

Takes into account, among others: 2006/42/EU, 2014/35/EU, 2014/30/EU, 2011/65/EU, EN ISO 12100, EN 60204-1, etc.

CE marking and consulting for laboratory equipment

CE marking and consulting for laboratory equipment

In the context of an upcoming ISO 45001 certification, easyCE supported a medical technology manufacturer with the CE documentation for a specialized testing and calibration machine for insufflators in the laboratory sector. Our specialists developed integrated documentation that covers both the CE requirements and the occupational health and safety aspects according to ISO 45001. Particular attention was paid to the safety requirements for handling various hose systems and connections, which can vary depending on the insufflator model.

Takes into account, among others: 2006/42/EU, 2014/35/EU, 2014/30/EU, 2011/65/EU, EN ISO 12100, EN 60204-1 etc.

CE marking for electrical equipment in medical laboratories

CE marking for electrical equipment in medical laboratories

As part of the ISO 45001 certification preparation process, easyCE supported a manufacturer of electrical laboratory equipment in the correct classification and CE conformity of its products. Our experts carried out a precise analysis to distinguish between medical devices and electrical equipment in order to ensure correct classification in terms of occupational health and safety. This clarity was crucial for the ISO 45001 requirements regarding hazard identification and risk assessment in the workplace. Successful documentation and conformity assessment enabled the customer to operate its laboratory equipment in full compliance with occupational health and safety guidelines and to pass the ISO audit without any objections.

Takes into account, among others: EN 55032, EN 55035, EN 60335-1 etc.

CE marking for test station for low-pressure units

CE marking for test station for low-pressure units

In the run-up to an ISO 45001 occupational health and safety audit, easyCE supported an industrial company in compiling CE documentation for an internal test bench for low-pressure units in accordance with occupational health and safety regulations. Our experts first analyzed the regulatory classification of the test bench and were able to prove through precise measurements that the Pressure Equipment Directive was not applicable. This clarification was crucial for the correct risk assessment within the framework of the ISO 45001 management system. The CE documentation subsequently created took particular account of occupational health and safety aspects such as operational safety and emergency procedures. This enabled the customer not only to demonstrate CE conformity, but also to pass its ISO 45001 certification without any deviations in the area of work equipment.

Takes into account, among others: 2006/42/EG, EN ISO 12100, EN 60204-1, EN ISO 4414, EN ISO 13849-1 etc.

Learn more about our project references and success stories

Get UKCA-marking done in 3 simple steps

Step 1

Request expert opinion

Ask for our expert opinion free of charge and find out what is necessary for the UKCA marking of your product. Be prepared to describe your product in broad terms.

Step 2

Receive our offer

If your product is subject to UKCA marking, we offer you our support with the UKCA marking and all accompanying measures. We will be happy to explain necessary steps on the phone.

Step 3

We get it done

When you place an order, you will be assigned your own personal UKCA expert who will carry out your UKCA marking and accompany you throughout the entire process. Your expert will also be at your side after the UKCA marking has been successfully completed.

Get UKCA-marking done, worry-free

+49 7248 45230405

Trust the experts of product safety and conformity

A picture of Willy Lebherz small

Willy Lebherz - Founder and Managing Director of easyCE

  • Expert in product safety and conformity since 1995
  • Recipient of the "Medal of the Order of Merit of the Federal Republic of Germany", awarded in 1983 by the then Federal President Carl Carstens
  • Master of measurement and control technology
  • Captain (ret.), Project Officer for Technical Logistics in the Army Material Office and Chief of the Telecommunications Repair Company

easyCE is a digital, dynamic engineering office with a focus on product safety and product conformity - especially CE-marking. We support manufacturers, operators and dealers in designing products safely and offering them on the market in compliance. We are a "full-service provider" and can take over the entire conformity assessment process for you if you wish. To do this, we support you in carrying out risk assessments, researching standards, product analyses, developing suitable safety precautions, preparing user-friendly technical documentation, coordinating tests and all other accompanying measures. easyCE was founded in southern Germany, but is now active globally.

We know what you need to do to get UKCA-marking done, worry-free.