This workflow helps decide whether an electrical or electronic item is outside EMC scope, EMC , a fixed installation, or specific apparatus for a fixed installation.
The output is a cited scope record that explains the intended use, market-placement facts, applicable overlap rules, EMC assessment route, and evidence file.
The EU EMC Directive has applied from 20 April 2016 to equipment, meaning or fixed installations. Apparatus is a finished appliance or combination supplied as one functional unit for an end-user when it can generate electromagnetic disturbance or its performance can be affected by that disturbance. Scope triage should first classify the item, check exclusions and more specific EU rules, and identify the evidence needed for the chosen route before a test lab is booked.
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Section 1
Start with market-placement and intended-use facts
Record the facts that decide whether the EMC Directive is even the right instrument: what the item is, whether it has electrical or electronic parts, who will use it, whether it is supplied on the Union market, and whether it is put into service at a fixed site.
For , placing on the market is the first making available of that apparatus on the Union market. The Directive also looks at equipment when it is put into service, properly installed, maintained, and used for its intended purpose.
Describe the item as sold or supplied: finished appliance, combination of finished products, component or sub-assembly for end-user incorporation, mobile installation, site installation, or specific for one fixed installation.
Write the intended use and electromagnetic environment in product language: industrial cabinet, residential lighting controller, plug-in card, power supply, mobile LED wall, plant control system, or another concrete use case.
Capture the commercial fact pattern: first EU supply, later distribution, import from a third country, own-use construction, trade-fair demonstration, or installation at a predefined location.
Keep a short conclusion that says whether the item is being assessed as , fixed installation, specific apparatus for a fixed installation, outside scope, or deferred pending more facts.
Defines equipment, apparatus, fixed installation, making available on the market, placing on the market, and the intended-purpose condition for making available or putting into service.
‘equipment’ means any apparatus or fixed installation
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Section 2
Separate apparatus from fixed installations
Classify as when the item is a finished appliance or combination made available as a single functional unit, intended for the end-user, and liable to generate electromagnetic disturbance or be affected by it. Components or sub-assemblies can also be treated as apparatus when they are intended for incorporation into apparatus by the end-user and have relevant EMC behaviour.
Classify as a fixed installation when several types of , and possibly other devices, are assembled, installed, and intended for permanent use at a predefined location. A mobile installation is not treated as a fixed installation just because it contains multiple items; the EMC guidance treats mobile installations as apparatus.
route: apply essential requirements, conformity assessment, EU declaration of conformity, CE marking, identification, traceability, and user information where the Directive requires them.
Fixed-installation route: do not close the file with CE marking or an EU declaration of conformity for the installation itself; fixed installations still need to meet essential requirements and be installed using good engineering practices and manufacturer instructions.
Specific- route: if the apparatus is intended only for a particular fixed installation and is otherwise not commercially available, record the fixed installation, EMC characteristics, identifying details, and incorporation precautions before relying on the fixed-installation-specific exception.
Escalate when a supplier calls something a component, kit, panel, skid, or installation but the facts show it is supplied as a single functional unit to an end-user.
Supports the apparatus and fixed-installation definitions and the separate conformity-assessment obligations for apparatus.
intended for the end-user
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Section 3
Handle inherently benign and borderline equipment carefully
The Directive excludes equipment whose inherent physical characteristics make it incapable of creating excessive electromagnetic emissions and able to operate without unacceptable degradation under the disturbance normally expected for its intended use. Both sides of that test matter: emissions and immunity.
A borderline conclusion should be documented, not assumed from a product label. The Commission guide gives examples such as cables and cabling, batteries and accumulators without active electronic circuits, headphones without active electronic parts, and simple resistive loads. Those examples are not automatic exclusions: added electronics, switching, filtering, amplification, radio functions, or installation-dependent behaviour can change the analysis.
Write the benign-equipment rationale in engineering terms: no active electronics, no automatic switching, no source likely to generate high-frequency disturbances, and no normal-use susceptibility that would cause unacceptable degradation.
Do not rely on an inherently benign conclusion for a whole fixed-installation category without site-specific reasoning; fixed-installation benignness is case-specific.
If the item is not inherently benign, continue triage instead of treating the absence of a harmonised standard as an exclusion.
When a reduced test approach is used because phenomena are physically irrelevant, keep the technical explanation with the assessment record.
Contains the legal exclusion for equipment whose inherent physical characteristics are benign for emissions and immunity in normal intended use.
it operates without unacceptable degradation
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Section 4
Check the named exclusions before closing scope
Besides inherently benign equipment and requirements governed more specifically by other Union legislation, Article 2 names several exclusions. These include specified aviation equipment within Regulation (EU) 2018/1139 when intended exclusively for airborne use, radio equipment used by radio amateurs unless made available on the market, and custom-built evaluation kits destined for professionals to be used solely at research and development facilities for those purposes.
Apply each exclusion to the actual supply and use facts. A commercially supplied development board is not excluded merely because a buyer may evaluate it, and amateur-radio equipment made available on the market does not qualify for the amateur-use exclusion. Kits of components assembled by radio amateurs and equipment modified by and for their own use are not treated as market-available equipment for that exclusion.
Record the exact exclusion, the facts that satisfy every condition, the person responsible for the conclusion, and the evidence retained.
For an evaluation kit, document that it is custom-built, destined for professional users, and used solely at research and development facilities for research and development purposes.
For radio-amateur equipment, distinguish own-use construction or modification from equipment made available on the market.
If only one requirement is governed more specifically by another Union act, document the remaining EMC Directive requirements instead of treating the whole product as excluded.
Article 2 sets the civil-aviation, radio-amateur, inherently benign, custom-built evaluation-kit, and more-specific-Union-legislation scope rules.
Recommended next step
Turn EMC scope triage into a release-ready evidence record
Use the scope, overlap, standards, and evidence questions on this page to prepare a concise EMC file before product release, supplier review, or authority response.
Check overlap with RED, LVD, Machinery, and other product rules
The EMC Directive stops applying to requirements that are wholly or partly laid down more specifically by other Union legislation from the date that legislation applies. Scope triage therefore needs an overlap check before selecting the EMC route.
Radio equipment generally moves the EMC aspects into the Radio Equipment Directive (RED) route. Wireline terminal equipment without a radio function can remain under the Low Voltage Directive (LVD) and EMC Directive when otherwise in scope. Functional-safety effects of electromagnetic disturbance may be handled by safety legislation such as Machinery or Low Voltage rules rather than by the EMC Directive alone.
Radio check: identify any intentional radio transmitter, receiver, radio-determination function, wireless module, or product that receives radio waves; do not treat radio equipment as ordinary EMC without checking RED scope.
LVD and Machinery check: separate electromagnetic compatibility from electrical safety or machinery functional-safety claims, because a product can need EMC evidence and also safety evidence under another EU act.
Medical, marine, vehicle, aviation, measuring, and sector-specific equipment may have more specific rules for some or all EMC requirements; record the exact act that changes the EMC answer.
If multiple EU acts require an EU declaration of conformity for the same , keep the act list and publication references aligned in the declaration package.
Supports the rule that the EMC Directive does not apply to requirements laid down more specifically by other Union legislation.
more specifically by other Union legislation
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Section 6
Produce an EMC scope evidence pack
Close triage with evidence that another reviewer can inspect without reconstructing the reasoning. Show the classification, exclusions considered, overlap conclusion, standards position, assessment route, and release consequence.
For , the evidence file should connect the scope conclusion to the technical documentation, conformity assessment route, EU declaration of conformity, CE marking, traceability information, instructions, and any restrictions for intended use or residential environments. For fixed installations, it should instead identify the responsible installation record, site borderlines, interfaces, good engineering practices, manufacturer instructions, and any specific-apparatus documentation.
Scope record: product identifier, hardware and software revision where relevant, intended purpose, electromagnetic environment, market-placement facts, and or fixed-installation classification.
Exclusion record: electrical/electronic-part check, inherently benign analysis, custom-built evaluation-kit status if relevant, radio-amateur or sector-specific exclusions, and more-specific-legislation conclusion.
Assessment record: harmonised standards used, standards not used or only partly used, other technical specifications, EMC phenomena considered, omitted tests with technical justification, and residual restrictions.
Release record: EU declaration of conformity status, CE marking status for , fixed-installation documentation status, owner for unresolved assumptions, and authority-response location for the supporting file.
Close with one explicit branch: in-scope ; in-scope fixed installation; Article 19 specific apparatus; excluded with every condition evidenced; governed wholly or partly by named more specific Union legislation; or blocked pending named facts. Set a reassessment trigger for product, intended-use, supply-model, installation, radio-function, vehicle-fitment, standards, or legal changes.
Supports the apparatus documentation, conformity assessment, EU declaration, CE marking, identification, instructions, and authority-response evidence points.
Primary legal source for EMC scope, apparatus and fixed-installation definitions, exclusions, intended use, placing on the market, essential requirements, conformity assessment, CE marking, and technical documentation.
Defines equipment, apparatus, fixed installation, making available on the market, placing on the market, and the intended-purpose condition for making available or putting into service.
Supports the apparatus and fixed-installation definitions and the separate conformity-assessment obligations for apparatus.
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Contains the legal exclusion for equipment whose inherent physical characteristics are benign for emissions and immunity in normal intended use.
Article 2 sets the civil-aviation, radio-amateur, inherently benign, custom-built evaluation-kit, and more-specific-Union-legislation scope rules.
Supports the rule that the EMC Directive does not apply to requirements laid down more specifically by other Union legislation.
Supports the apparatus documentation, conformity assessment, EU declaration, CE marking, identification, instructions, and authority-response evidence points.
"‘equipment’ means any apparatus or fixed installation"