Regulation (EU) 2023/988 applies as the EU general safety rule for consumer products placed or made available on the Union market, including targeted online and distance sales.
This page helps document whether a product is covered, excluded, partly handled by sector-specific Union law, or caught because it has moved into consumer use.
The GPSR has applied since 13 December 2024. Start the scope analysis with the , placement date, and sales facts. Decide whether the item is a consumer product placed or made available on the EU market, including through a targeted distance-sales offer, whether an exclusion applies, and whether another Union law regulates the same risk.
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Section 1
What products are in scope
The GPSR covers products placed or made available on the market where no specific Union law regulates the same -safety objective. A product can be in scope even if it is supplied for free, supplied during a service, interconnected with another item, or originally intended for professional use but likely to be used by consumers under reasonably foreseeable conditions.
The scope decision should identify the item, intended users, reasonably foreseeable consumer users, supply route, EU market availability, and whether the is new, used, repaired, or reconditioned. Services themselves are outside the product scope, but products made available to consumers in the context of a service can still be covered.
Treat a as potentially covered when it is intended for consumers or likely to be used by consumers, even if the design brief says professional use only.
Include products supplied in a service setting when consumers are directly exposed to the , unless the item is transport equipment directly operated by the service provider.
Separate the -safety scope decision from later duties such as risk analysis, technical documentation, online listing data, accident reporting, or recall notices.
For stock placed on the market before 13 December 2024, check Article 51 separately. It protects further making available only where the was covered by and conformed to Directive 2001/95/EC before that date; acquisition or listing after the date does not by itself prove the transition applies.
Use the scope record to connect each product, sales channel, operator role, exclusion, and Union-law overlap decision to the evidence your product, regulatory, legal, and marketplace teams need later.
A offered online or through another distance-sales channel is treated as made available on the EU market when the offer targets consumers in the Union. Accessibility of a website from an EU Member State is not enough on its own; the scope record should capture targeting signals such as shipping destinations, order language, payment methods, Member State currency, and Member State domain use.
For an in-scope online offer, GPSR listing evidence should show the manufacturer name and contact details, the EU responsible person when the manufacturer is not established in the Union, identifiers including a picture, and any warning or safety information required on the product, packaging, or accompanying documents.
Capture screenshots or exports of listings as they appeared to EU consumers, including language, currency, delivery options, seller identity, and product identifiers.
Record whether the channel is a direct sale, marketplace listing, fulfilment-service model, or mixed role, because the same entity can be an online marketplace provider and an economic operator for the same .
When the is sold through an online marketplace, verify that the listing process can collect and display the GPSR product-safety and traceability information required for online offers.
GPSR expressly covers products placed or made available on the market whether they are new, used, repaired, or reconditioned. That means resale, refurbishment, repair-return, outlet, and reconditioned-stock programs need a -level safety and traceability view when they re-enter a commercial supply chain.
The main carve-out is narrow: products to be repaired or reconditioned before use are outside this rule only when they are clearly marked as such. The scope file should keep the listing text, label, invoice language, or intake record that shows the was presented as requiring repair or reconditioning before use.
Do not assume second-hand status removes GPSR scope; decide whether the item is being made available for consumer use in a commercial activity.
For refurbished or repaired goods, keep the repair scope, changed components, safety checks, warnings, and identifiers tied to the specific batch or serial number.
If a is sold as repair-only, keep the clear marking evidence and prevent consumer-facing copy from implying that the item is ready for safe use.
Article 2 excludes medicinal products, food, feed, living plants and animals, GMOs and genetically modified microorganisms in contained use, plant and animal reproductive products listed in the provision, animal by-products and derived products, plant protection products, specified transport equipment directly operated by a service provider, certain aircraft, and antiques.
For products covered by specific Union safety requirements, GPSR applies only to aspects, risks, or risk categories those requirements do not cover. Products subject to Union harmonisation legislation need an additional chapter-level check: current Article 2 excludes Chapter II for covered risks and switches off Chapter IIa, Chapter III Section 1, and Chapters V, VII, and IX to XI. Chapter IIa contains emergency procedures for designated crisis-relevant goods. Other provisions, including distance-sales, accident, online-marketplace, Safety Gate, recall, and remedy rules, may still apply according to their terms and the same-objective test.
List every claimed exclusion with the facts that support it; avoid broad labels such as medical, food-adjacent, antique, or professional without evidence.
For CE-marked or otherwise harmonised products, map each safety risk to the sector law first, then apply the Article 2 chapter exclusions before assigning any residual GPSR duty.
Keep the overlap matrix at risk level: electrical, chemical, mechanical, connected-, child-use, warning, recall, online listing, and accident-reporting issues may be governed by different instruments.
A defensible GPSR scope decision should connect the facts to the operator role. Where GPSR Chapter III, Section 1 applies, manufacturers need an internal risk analysis and technical documentation before placing products on the market. Importers must check the manufacturer documentation, product identification, and manufacturer contact information before placing a product on the market. Distributors must verify required product, manufacturer, importer, instruction, and safety-information checks before making the product available.
Where Article 16 applies to a covered placed on the Union market, it requires an economic operator established in the Union responsible for the relevant Regulation (EU) 2019/1020 tasks. For higher-risk or complex products, the evidence file should also include documented checks that the product matches the technical documentation and required identification, contact, instruction, and safety-information data.
Reassess scope when the intended user, sales channel, EU targeting, condition, labelling, service model, or applicable sector law changes. A professional product can move into foreseeable consumer use, a repair-only item can be relisted as ready to use, and a previously domestic offer can begin targeting EU consumers.
Keep the scope memo, role map, EU responsible-person details, identifiers, listing evidence, and any exclusion or Union-law-overlap matrix with the product file.
For manufacturer evidence, retain the risk analysis, technical documentation, standards or other safety elements applied, test reports, warnings, instructions, and change history.
For importer, distributor, and marketplace evidence, retain pre-sale checks, supplier confirmations, listing screenshots, consumer-facing warnings, complaint and accident handoff records, and any corrective-action decision.
Articles 9 to 16 support the evidence guidance for manufacturer technical documentation, importer and distributor checks, cooperation with authorities, traceability, and the EU-established responsible economic operator.