The LVD (Directive 2014/35/EU) covers electrical equipment designed for use with a voltage rating between 50-1000 V AC or 75-1500 V DC, unless an Annex II exclusion or a more specific product-law route applies.
By Sorena AIBased on official EU sourcesNo signup required
Quick scan
LVD
Classify the equipment
Start with the product boundary, voltage rating, intended use, foreseeable installation, and whether the item is finished electrical equipment, a component, machinery, radio equipment, or equipment within a specific Annex II exclusion. A component or adjacent product-law category is not automatically outside the LVD.
Build the safety case
Translate Annex I into product-specific evidence: risk analysis, design drawings, circuit and component information, standards applied in full or in part, other specifications, examinations, calculations and test reports.
Prepare CE release records
Under Annex III , the manufacturer establishes technical documentation, keeps production aligned with it, draws up the EU DoC and affixes CE marking before placing compliant equipment on the market.
Review this hub before design freeze, supplier onboarding, importer review, distributor listing, or first EU placement. Reopen the record after a material design, component, firmware, intended-use, installation, supplier, standards, or market-role change, and when complaints, test failures, corrective action, or an authority request challenge the existing conclusion.
Key dates
50-1000 V
AC scope
75-1500 V
DC scope
Annex I
Safety objectives
Annex III
Internal control
What this hub helps you check
Voltage scope and exclusions
Confirm the AC or DC voltage rating, then test Annex II exclusions and adjacent regimes such as EMC, RED or Machinery where the product design points there.
Safety objectives and standards
Map Annex I hazards to design controls, intended use, installation and maintenance assumptions, , deviations and test evidence.
Release evidence and operator duties
Use Annex III : the manufacturer owns the LVD conformity decision, technical documentation, EU Declaration of Conformity, CE marking, production controls, and 10-year retention. Importers and distributors perform their own pre-supply checks and post-market actions; the LVD route does not require a notified body.
Classify voltage scope
Map Annex I evidence
Prepare DoC + CE
Publication details
Editorial metadata for this artifact
Author
Sorena AI
Published
Feb 21, 2026
Updated
Jul 25, 2026
Directive 2014/35/EU has applied since 20 April 2016. Start with the rated-voltage and product boundary, then identify the market event and actor: is the first supply of the equipment in the EU, while is any commercial supply for distribution, consumption, or use, including supply free of charge. Connect the manufacturer, importer, distributor, or authorised-representative role to the Annex I safety evidence, release checks, retention duties, and post-market action it controls. The Directive and the Member State laws that transpose it govern the legal duties; Commission guidance helps interpretation but is not binding.
Focused LVD guidance
Check the standard behind your safety case
Use the EU record to decide whether a standard supports the Low Voltage Directive (LVD) safety objectives and what must change when a cited standard is restricted, replaced, or withdrawn.
Use LVD harmonised standards correctly
Check the exact standard, edition, amendment, restriction, and withdrawal date in the EU , the official list of standards cited for the LVD. Using a cited standard is voluntary. It creates a only for the safety objectives and conditions covered by that citation; the manufacturer must address any remaining hazards separately.
Track the directive text, Commission LVD guidance, harmonised-standard publications and withdrawals, technical-documentation updates, EU DoC updates, CE marking checks and market-surveillance evidence for each product model.
Loading timeline...
Recommended reading path
Choose the next LVD decision
New to the LVD? Establish the product boundary, rated voltage, exclusion status, and economic-operator role first. If those decisions are documented, jump to safety evidence, conformity release, standards maintenance, post-market controls, or a product-law comparison.
1
Start here: scope and routing
Decide whether the item is electrical equipment designed for the LVD voltage bands, whether an Annex II exclusion fits, and whether RED, machinery law, or another route changes the legal file.
Translate Annex I hazards into product-specific controls, then assign manufacturer, importer, distributor, and authorised-representative duties without treating a supplier certificate as the finished-product safety case.
Build the Annex III internal-production-control record: standards rationale, risk analysis, design and test evidence, technical documentation, EU declaration of conformity, CE marking, and production-release controls.
Keep the conformity basis current after release by monitoring OJEU citations and withdrawals, retention clocks, complaints, corrective action, authority requests, and Member State enforcement exposure.
Separate LVD safety evidence from EMC, RED, RoHS, machinery, and horizontal market-surveillance obligations while keeping shared product identity and release records aligned.
Use the FAQ for direct answers about thresholds, batteries, chargers, components, household appliances, importers, instructions, spare parts, and standards withdrawal.
Turn LVD scope and evidence into owned release work
This hub helps route LVD work by product model, voltage rating, intended use, standards set, operator role and EU market path. Assessment Autopilot can convert the release evidence into owned tasks; Research Copilot can support cited questions about scope, exclusions, standards, documentation and overlap with EMC, RED or Machinery.
What this unlocks
Start with the equipment boundary, voltage rating, intended use, installation context, EU market path and economic operator responsible for placing or making the product available.
Use Assessment Autopilot to request the risk analysis, Annex I safety mapping, standards list, deviations rationale, test reports, instructions, traceability details, technical documentation, EU DoC and CE marking review.
Use Research Copilot for cited questions about Annex II exclusions, harmonised-standard withdrawal, manufacturer versus importer duties, distributor checks, market-surveillance requests and product-law overlaps.
Keep engineering, supplier, test-lab, quality, importer, distributor, release, corrective-action and authority-response records connected to the same equipment file.