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CE marking vs UKCA in 2026

Last reviewed: October 2026 · Sources listed at the end of this page.

UKCA — "UK Conformity Assessed" — is the conformity mark Great Britain created after leaving the European Union. It was designed as a domestic replacement for CE marking, applying essentially the same technical requirements through legislation retained from EU law. In practice, the replacement never happened. After a series of postponed deadlines, Great Britain now recognises current EU requirements, including CE marking, with no end date for products under 21 product regulations, and UKCA survives as an optional alternative for those categories rather than a requirement. Other sectors follow their own rules. Some of them still accept CE marking on separate terms (construction products, medical devices, cableways); others do not use it at all (marine equipment, transportable pressure equipment, drones).

At a glance. UKCA is Great Britain's conformity mark and CE remains accepted alongside it for most products. Status at 31 October 2026: no end date for CE recognition under the 21 regulations. A UK approved body is not needed if the product is lawfully CE marked under those regulations. Key dates: 20 January 2027, when GB rules start to accept machinery meeting the EU Machinery Regulation; 21 October 2026, when the government said it will legislate for long-term recognition of CE-marked medical devices.

This page sets out how the two marks relate in 2026, which sectors sit outside the recognition arrangement, and how Northern Ireland differs from Great Britain. For what CE marking itself signifies, see what is CE marking?

From Brexit to indefinite recognition

The UK left the EU on 31 January 2020 and remained inside the single market until the end of the transition period on 31 December 2020. From 1 January 2021, Great Britain (England, Wales, and Scotland) operated its own product compliance regime based on EU law as retained at exit, with UKCA as its conformity mark and "approved bodies" taking the role of EU Notified Bodies.

CE marking was originally to be accepted in Great Britain only for a short transitional period. That period was extended repeatedly:

DateEvent
1 January 2021UKCA marking becomes available; CE marking continues to be accepted in Great Britain on a transitional basis.
2021–2022The original end-of-2021 deadline for mandatory UKCA is extended, first to the end of 2022, then to the end of 2024.
August 2023The UK Government announces that CE marking will continue to be recognised indefinitely for most product categories overseen by the Department for Business and Trade.
2024The Product Safety and Metrology etc. (Amendment) Regulations 2024 (SI 2024/696) continue recognition of EU requirements, including CE marking, across a broad set of product regulations, with effect from 1 October 2024.
21 July 2025The Product Regulation and Metrology Act 2025 receives Royal Assent. It is enabling legislation: it lets ministers make product regulations, and later instruments rely on it. CE recognition under the 21 regulations continues to rest on the 2024 Regulations.
January 2026The Construction Products (Amendment) Regulations 2025 come into force, supporting continued CE recognition for construction products.
22 July 2026The Supply of Machinery (Safety) (Amendment etc.) and the EU Machinery Regulation (Enforcement etc. in Northern Ireland) Regulations 2026 (SI 2026/867) are made, in force from 20 January 2027.
21 October 2026The government confirms it will legislate to recognise CE-marked medical devices and IVDs certified under the EU MDR and IVDR indefinitely.

The practical result: for the great majority of CE-marked products — machinery, electrical and electronic equipment, toys, PPE, pressure equipment, and the other categories listed below — a product that lawfully carries CE marking can be placed on the market in Great Britain without any UKCA marking, and no end date has been set.

The 21 product regulations covered by CE recognition

Continued CE recognition in Great Britain applies to products within the scope of 21 GB product regulations, which broadly mirror the EU harmonisation acts. The categories include:

The list above follows the gov.uk guidance "Placing manufactured goods on the market in Great Britain", last updated in May 2024. The government's March 2026 document "Product regulations by sector" is the newer overview, sector by sector. Where a product sits at the edge of a category, the applicable GB regulation, not this summary, is decisive.

Recognition covers conformity assessment, not just the mark. Where CE recognition applies, Great Britain accepts conformity assessment carried out under the EU rules — including certificates issued by EU Notified Bodies. A manufacturer does not need to repeat testing with a UK approved body to sell a CE-marked product in Great Britain in these categories.

UKCA in 2026: a valid, optional alternative

UKCA marking has not been abolished. For the categories covered by CE recognition, a manufacturer may choose to affix UKCA instead of, or alongside, CE marking for the GB market. Reasons some manufacturers keep UKCA include existing certification with UK approved bodies, retail customer requirements, or a wish to hedge against future divergence. But there is no regulatory obligation to use it in those categories, and we found no announced date on which CE recognition ends. Current guidance also allows a UKCA marking to go on a label or accompanying document until 11pm on 31 December 2027.

Where UKCA is used, the GB rules broadly track the familiar CE mechanics: the mark is affixed by the manufacturer, a UK declaration of conformity is drawn up (analogous to the EU Declaration of Conformity), "designated standards" give a presumption of conformity in the way harmonised standards do in the EU, and third-party assessment, where a module requires it, is performed by a UK approved body whose number accompanies the mark.

Sectors following separate UK regimes

The 21-regulation arrangement is not universal. The table summarises the other main sectors, using the government's March 2026 overview, updated for later decisions.

SectorGB positionCE accepted in GB?
Medical devices and IVDsUK MDR 2002, MHRAYes, for now on statutory end dates; legislation for long-term recognition promised
Construction productsConstruction Products Regulation as it applies in GB, MHCLGYes, no fixed end date; any change subject to at least two years' transition
Cableway installationsCableway Installations Regulations 2018, DfTYes
Rail interoperability constituentsRailways (Interoperability) Regulations 2011, DfTNo GB marking; EU declarations accepted where the EU and GB requirements are equivalent
Marine equipmentMerchant Shipping (Marine Equipment) Regulations 2025, MCANo: Red Ensign mark for UK-registered ships
Transportable pressure equipmentCarriage of Dangerous Goods regulations, DfTNo: rho mark in GB
Uncrewed aircraftAssimilated Regulation (EU) 2019/945, DfT and CAANo: UK0 to UK6 class marks
BatteriesBatteries and Accumulators Regulations 2008, DefraNo GB marking required

Medical devices

Medical devices in Great Britain are regulated under the Medical Devices Regulations 2002 (UK MDR 2002), as amended, overseen by the MHRA — not under the EU Medical Devices Regulation (EU) 2017/745. Under the Medical Devices (Amendment) (Great Britain) Regulations 2023, CE-marked devices are accepted in Great Britain until 30 June 2028 (or earlier certificate expiry) for devices under the MDD or AIMDD, and until 30 June 2030 for devices under the IVDD (or earlier certificate expiry), the EU MDR or the EU IVDR. On 21 October 2026, after a consultation that ran from 16 February to 10 April 2026, the government said it intends to legislate to recognise CE-marked devices certified under the EU MDR and IVDR indefinitely, and to align GB transitional arrangements for MDD devices with EU timelines. That is a stated intention: until the amending regulations are made, the statutory dates above still apply. Manufacturers must still appoint a UK Responsible Person where required, register devices with the MHRA, and meet GB post-market surveillance rules. Check current MHRA guidance before relying on any date.

Construction products

Construction products follow a separate GB framework based on the retained Construction Products Regulation, while the EU regime migrates to Construction Products Regulation (EU) 2024/3110. The government committed in September 2024 to keep recognising CE marking for construction products, subject to wider reform, with at least two years' transition before any later change. The Construction Products (Amendment) Regulations 2025 came into force in January 2026, and a reform white paper followed in February 2026. Designated standards are mandatory under the GB construction products rules, unlike most other sectors.

Rail, marine equipment, transportable pressure equipment, and cableways

Products outside any harmonisation act

These are governed in GB by the General Product Safety Regulations 2005, while the EU applies the General Product Safety Regulation (EU) 2023/988, applicable since 13 December 2024. The two regimes have diverged. On 31 March 2026 the UK opened a consultation, closed on 23 June 2026, on replacing the 2005 Regulations under the 2025 Act, with new duties for online marketplaces and civil penalties. We found no government response as of 31 October 2026, so the 2005 Regulations remain the law.

Northern Ireland: EU rules under the Windsor Framework

Northern Ireland applies EU product rules under the Windsor Framework. Products placed on the market in Northern Ireland must comply with the applicable EU harmonisation legislation and carry CE marking where the EU acts require it — UKCA alone is not valid there.

Where mandatory third-party conformity assessment is carried out by a UK-based notified body rather than an EU Notified Body, the product carries the UKNI marking alongside the CE marking. Two consequences follow:

Qualifying Northern Ireland goods benefit from unfettered access to the rest of the UK market, so a qualifying product lawfully on the market in Northern Ireland can generally also circulate in Great Britain. From 20 January 2027, SI 2026/867 also applies the EU Machinery Regulation's enforcement rules in Northern Ireland.

Divergence: the risk to watch

CE recognition in Great Britain means GB currently accepts compliance with the EU requirements, but the two statute books are no longer mechanically linked, so recognition has to be renewed by UK legislation when EU law changes:

The Product Regulation and Metrology Act 2025 gives UK ministers powers to make product regulations, which is how recognition can follow, or stop following, EU changes over time. See 2025–2026 changes for the moving parts on the EU side.

Practical guidance for manufacturers selling in both markets

  1. Classify your product first. Establish which EU acts apply (does my product need CE marking?) and whether the corresponding GB regulation is one of the 21 covered by CE recognition.
  2. If it is covered: complete the CE marking process once. CE marking then serves the EU, the EEA, and Great Britain. UKCA is optional; dual marking is permitted if you want it.
  3. If it is not covered: use the sector table above. CE can serve for construction products, cableways, and (with MHRA registration and a UK Responsible Person where needed) medical devices. Marine, transportable pressure equipment, and uncrewed aircraft need GB-specific marking, so plan a separate compliance track.
  4. Mind the operator roles. An EU-established manufacturer selling into GB will typically have a UK importer. For goods imported from the EEA, and in some cases Switzerland, importer details may go in an accompanying document or on the packaging until 11pm on 31 December 2027; a UK manufacturer selling into the EU needs an EU-established economic operator under Article 4 of Regulation (EU) 2019/1020 for many categories (see importing from non-EU manufacturers and authorised representative).
  5. For Northern Ireland: follow EU rules; use an EU Notified Body if you want a single assessment valid EU-wide, since CE + UKNI is NI-only.
  6. Monitor divergence. Where an EU act is replaced, confirm how GB recognition treats the new EU requirements before relying on a single technical file for both markets. For machinery, SI 2026/867 answers that question from 20 January 2027.

Frequently asked questions

Is UKCA marking mandatory in 2026?

Not for products under the 21 GB regulations where CE recognition applies. A manufacturer may use CE, UKCA, or both. Sectors outside those regulations have their own rules, and some require GB-specific marking.

Can I sell a CE-marked product in Great Britain?

Usually yes. A product that lawfully carries CE marking under one of the 21 regulations can be sold in Great Britain without UKCA. You still need to meet GB duties such as importer identification.

Will CE-marked machinery still be accepted in GB after 20 January 2027?

Yes, on the conditions in SI 2026/867. From 20 January 2027, machinery meeting the EU Machinery Regulation can be placed on the GB market if it has the required technical documentation, conformity assessment, EU declaration, English instructions, and CE marking.

Are CE-marked medical devices recognised indefinitely in Great Britain?

Not yet in law. On 21 October 2026 the government said it intends to legislate for indefinite recognition of devices certified under the EU MDR and IVDR. Until then, the dates in the 2023 Regulations apply.

Does the 21 product regulations figure include every CE-marked product?

No. Medical devices, construction products, cableways, marine equipment, rail, transportable pressure equipment, and uncrewed aircraft are outside it, with their own arrangements.

Can a CE + UKNI product be sold in the EU?

No. UKNI means a UK-based notified body carried out the assessment for the Northern Ireland market. For the EU market, use an EU Notified Body.

Sources