Follow us
Get in touch!

Unit 6 Stoneacre
St James Retail Park
Grimbald Crag Close
Knaresborough
HG5 8PJ
A white background with the Haredata electronic logo

FRIWO | UK

The New UKCA (UK Conformity Assessed) Marking

Ben Winstanley • December 15, 2020

The UKCA (UK Conformity Assessed) marking is a new UK product marking that will be used for goods being placed on the market in Great Britain (England, Wales and Scotland). 

It covers most goods which previously required the CE marking.

Countdown to implementation

Days
Hours
Minutes
Seconds
Countdown finished!

Grace Period

Days
Hours
Minutes
Seconds
Countdown finished!

When does this new standard come into action?

The UKCA mark can be applied to products sold in the UK from 1st January 2021. 


There will be a grace period of 1 year to allow manufacturers to update existing product labels accordingly.

During this grace period, it will be acceptable for products that are sold in the UK to only bear the CE mark.


From 01 January 2022, all products sold in the UK will be required to carry the UKCA mark.

Additionally, products sold in Northern Ireland requiring a UKCA mark one year later, on 1 January 2023.


In some cases you will need to apply the new UKCA marking to goods being sold in Great Britain immediately from 1 January 2021.**

You are encouraged to be ready to adopt the UKCA marking as soon as possible!


The CE marking will only be valid in Great Britain for areas where GB and EU rules remain the same. If the EU changes its rules and you CE mark your product on the basis of those new rules you will not be able to use the CE marking to sell in Great Britain even before 31 December 2021

When to use the UKCA Marking?

**You will need to use the new UKCA marking immediately after 1 January 2021 if all of the following apply. Your product:


  • is for the market in Great Britain
  • is covered by legislation which requires the UKCA marking
  • requires mandatory third-party conformity assessment
  • conformity assessment has been carried out by a UK conformity assessment body and you haven’t transferred your conformity assessment files from your UK body to an EU recognised body before 1 January 2021


This does not apply to existing stock, for example if your good was fully manufactured and ready to place on the market before 1 January 2021.

In these cases your good can still be sold in Great Britain with a CE marking even if covered by a certificate of conformity issued by a UK body.

Where to apply the UKCA Marking?

In most cases, you must apply the UKCA marking to the product itself or to the packaging. In some cases, it may be placed on the manuals or on other supporting literature. This will vary depending on the specific regulations that apply to the product.


The following general rules apply:


  • UKCA markings must only be placed on a product by you as the manufacturer or your authorised representative
  • when attaching the UKCA marking, you take full responsibility for your product’s conformity with the requirements of the relevant legislation
  • you must only use the UKCA marking to show product conformity with the relevant UK legislation
  • you must not place any marking or sign that may misconstrue the meaning or form of the UKCA marking to third parties
  • you must not attach other markings on the product which affect the visibility, legibility or meaning of the UKCA marking
  • the UKCA marking cannot be placed on products unless there is a specific requirement to do so in the legislation

Rules for using the UKCA image

You must make sure that:


  • if you reduce or enlarge the size of your marking, the letters forming the UKCA marking must be in proportion to the version set out (see right)


  • the UKCA marking is at least 5mm in height – *unless a different minimum dimension is specified in the relevant legislation


  • the UKCA marking is easily visible, legible (from 1 January 2023 it must be permanently attached)



Product areas covered by the UKCA marking

  • Toy safety
  • Recreational craft and personal watercraft
  • Simple pressure vessels
  • Electromagnetic compatibility
  • Non-automatic weighing instruments
  • Measuring instruments
  • Lifts
  • ATEX
  • Radio equipment
  • Pressure equipment
  • Personal protective equipment
  • Gas appliances
  • Machinery
  • Outdoor noise
  • Ecodesign
  • Aerosols
  • Low voltage electrical equipment
  • Restriction of hazardous substances


Products covered by the UKCA marking but have some special rules:


  • medical devices
  • rail interoperability
  • construction products
  • civil explosives

What are the differences between UKCA and CE marking?

Many of the differences between the two systems are administrative in nature and reflect that UKCA only applies in the UK and only requires information in English. This simplifies some aspects, such as where the technical information must be kept and which language applies.

Other differences relate to the separation of UK conformity assessment bodies from the EU Notified Body System.

What aspects are not changing?

Many facets are the same; the scope of products covered, technical requirements (essential requirements, standards) and conformity assessment procedures will all initially be alike. If your product is sold in both the EU and the UK, the technical file to show that it meets these requirements will also be the same.

What is the specific UK legislation that needs to be followed?

To implement the new regime, the UK government has issued several Statutory Instruments to amend current legislation.

The main regulations are The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019, which runs to 659 pages.

These regulations amend most of the UK CE marking regulations for products placed on the UK market and stipulate the UKCA mark.


Where a directive required CE marking and UK regulations were already detailed, the amendments are limited to:


  • replacing the CE mark with the UKCA mark, 
  • limiting applicability to products for the UK market, 
  • changing references to Notified Bodies to Approved Bodies, 
  • changing language references to English. 

What safety markings are required in other Countries?

Read our BLOG on it below

Be warned, one of the approvals listed is fake, can you spot it?!

CONTACT US

COMMENT ON THIS POST

SHARE THIS POST
While you're here, why not read some of our other blog posts?
We are 99% sure you'll learn something!
A group of Friwo FOX NEO Power Supplies
By Alex Chapman July 11, 2024
If you're wondering how o find the power power supply, check out this guide to help make your decision simple!
Medical devices in an operating theatre
By Alex Chapman July 11, 2024
Why is power so important for medical devices. Join us as we explore what makes power supplies, batteries and chargers so important for medical devices.
A group of DC connectors with USB Type-C, Magnetic connector, Barrel connector with inner pin
By Alex Chapman February 23, 2024
Join us for a deep dive into the pros and cons of Direct Current (DC) connectors. have a project that requires a DC connector? Find your perfect match here!
The UKCA Guide for manufacturers of technical products and medical devices
By Ben Winstanley November 18, 2021
Introduction
An exoskeleton object with the letter x on it
By Ben Winstanley October 6, 2021
INDEPENDENT POWER SUPPLY FOR MEDICAL EXOSKELETONS A FRIWO systems solution in practice Finally being able to walk again. ExoAtlet, the renowned medical technology company, wants to grant that exact wish to its patients with physical disabilities. The specially designed and built exoskeleton allows people who have been confined to a wheelchair to stand freely, and without assistance, for the first time since their disability – and not only stand, but walk! The “ExoAtlet II” skeleton allows the wearer to move at different speeds as well as across different types of terrain without being hindered by stairs or other obstacles.
Battery Charging
By Ben Winstanley May 12, 2021
Selection and operation of a battery charger
Switchmode Power Supplies vs Linear Power Supplies
By Ben Winstanley May 5, 2021
Switchmode Power Supplies vs Linear Power Supplies The vast majority of low voltage external power supplies sold globally these days are switching (switchmode) units, as opposed to the original Linear technology, which is only considered appropriate for certain niche markets due to it’s inability to meet required efficiency standards. In this article we will explore just some of the technical aspects & features and benefits of Switchmode topology vs Linear.
Micro USB Vs USB-C Comic Battle - Visual Created by Haredata Electronics
By Ben Winstanley January 28, 2021
The micro USB connector has been the most common connector for plug top devices for the last few years, but as with everything the times are changing. This is where the Type-C USB has started to step in, with more and more pieces of tech coming with a Type-C charger rather than the old favourite. So the question is why? If the old micro USB isn’t broken then why ‘fix’ it? 
What is MDR? The New Medical Device Regulation
By Ben Winstanley October 29, 2020
What is MDR? Medical Device Regulation MDR is a new regulation issued by the European Parliament and the council of medical devices. It is replacing previous medical device directives 90/385/EEC and 93/42/EEC. The requirements of the new regulation are more complex than previously and are different per product. The vast majority of products are subject to new labelling and documentation requirements, such as; • Requirements for a unique device identification number (UDI) • Traceability of products The new requirements specified by the MDR cover each role played by differing companies on the supply chain, meaning at each step there are new responsibilities to be aware of. When does the MDR come into play? The MDR was initially due to begin the transition in May of this year but due to the global pandemic it is has been postponed to 26th May 2021. This transition deadline has to be met by all companies and suppliers by the date. What does MDR mean for power supplies?
The word iec is written in the sand on the beach.
By Ben Winstanley October 27, 2020
From December 20, 2020, the IEC 62368-1 is set to take over from the IEC 60950-1 and IEC 60065 for the new standard for ICT and AV equipment. It brings together two separate standards linking terminologies and key engineering tenets, this new standard will become law and be used throughout Europe and USA. In Europe, the transition will be rapid and the expectation for all equipment to meet these new standards will be expected. Whereas, in the USA the transition will be slower starting with new submissions matching the standards and some existing products not having to be re-reviewed. Why the change? The IEC 62368-1 is a unified and smoother set of standards to follow internationally. It is here to revolutionise the approach for basic hazard safety, as new types of affordable products have emerged for use both leisurely and for business. Due to the constant changing state and technological advances blurs the lines between AV and ICT are blurred meaning the standards should begin to overlap
More Posts
Share by: