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ActiveInternational Standardupdate Standard Updated: July 2016fact_check Fact checked: Jun 28, 2026

Pressure Equipment Directive (2014/68/EU)

PED — Directive 2014/68/EU on the making available of pressure equipment

apartmentPublishing Organization:European Union

Standard Introduction

Pressure Equipment Directive (2014/68/EU) is an active standard published by European Union. It is commonly used across Machinery, Manufacturing, Energy, Chemical & Materials and applies in European Union, European Economic Area.

Use this page to review the official documentation, current status, and the certification or assessment bodies most commonly associated with Pressure Equipment Directive (2014/68/EU).

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Pressure Above 0.5 bar

Applies to pressure equipment and assemblies with a maximum allowable pressure greater than 0.5 bar — including refrigerant circuits in larger HVAC and refrigeration plant.

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Risk Categories I–IV

Classifies equipment by hazard (fluid group, pressure, volume) into categories that determine the conformity assessment route and Notified Body involvement.

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Notified Body Role

Higher categories require a Notified Body to assess design, manufacturing, and final inspection of the pressure equipment.

list_alt Key Elements

  • Scope: maximum allowable pressure PS > 0.5 bar
  • Fluid groups 1 (dangerous) and 2 (other)
  • Hazard categories I, II, III, IV
  • Conformity assessment modules by category
  • Sound engineering practice for the lowest category
  • Material and welding qualification requirements
  • CE marking and EU Declaration of Conformity

Who Needs to Comply?

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Manufacturers and importers of pressure equipment — vessels, piping, safety accessories, and pressurised assemblies — placed on the EU market, including refrigeration and air-conditioning systems above the pressure threshold.

Key Requirements

1

Classify the Equipment

Determine the hazard category from pressure, volume/dimensions, and fluid group to identify the applicable conformity assessment modules.

2

Design & Material Controls

Design for the relevant loads, qualify materials and welding procedures, and apply harmonised standards such as EN 378 (refrigerating systems) or EN 13445 (vessels).

3

Conformity Assessment

Engage a Notified Body where the category requires it for design examination, production quality assurance, or final inspection.

4

Documentation & Marking

Compile the technical file, draw up the EU Declaration of Conformity, and apply the CE marking with the Notified Body number where applicable.

Implementation Roadmap

1
Phase 1schedule Duration: 2-6 weeks

Define Pressure Equipment Directive (2014/68/EU) scope

Identify the pressure equipment and assemblies with maximum allowable pressure above 0.5 bar in scope, the legal or customer obligations that apply, accountable owners, affected products or services, jurisdictions, suppliers and evidence expectations. Confirm coverage for pressure equipment scope, fluid group, pressure and volume thresholds, hazard category, conformity module, Notified Body role, materials, joining, final assessment, technical file and CE marking.

2
Phase 2schedule Duration: 4-10 weeks

Assess obligations and gaps

Compare current design, operations and documentation against Pressure Equipment Directive (2014/68/EU). Review pressure equipment scope, fluid group, pressure and volume thresholds, hazard category, conformity module, Notified Body role, materials, joining, final assessment, technical file and CE marking, then prioritise gaps by safety, legal exposure, market-access impact, customer commitments, reporting deadlines and assurance readiness.

3
Phase 3schedule Duration: 8-24 weeks

Implement controls and evidence

Deploy the procedures, technical controls, testing, training, supplier controls, review gates and operating records needed for Pressure Equipment Directive (2014/68/EU). Maintain classification worksheets, design calculations, material certificates, welding qualifications, pressure-test records, final inspection records, Notified Body certificates, instructions and declarations of conformity as traceable evidence.

4
Phase 4schedule Duration: Ongoing

Review, verify and maintain

Run management review, internal checks, retesting or independent assessment where appropriate. Refresh the program when products, services, suppliers, standards, regulations, incidents, customer commitments or market-surveillance expectations change.

Compliance Checklist

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checklist Scope and accountability

checklist Controls and records

checklist Monitoring and assurance

Penalties & Enforcement

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Market surveillance authorities can prohibit sales, require recalls, and impose fines. Equipment failing pressure-safety requirements poses serious risk and attracts strict enforcement.

Frequently Asked Questions

Who needs Pressure Equipment Directive (2014/68/EU)?

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Pressure Equipment Directive (2014/68/EU) is relevant to organizations that design, manufacture, import, distribute, operate, certify, test or procure pressure equipment and assemblies with maximum allowable pressure above 0.5 bar. Exact applicability depends on the product or service scope, jurisdiction, role in the supply chain, customer commitments and the specific obligations triggered by the standard or regulation.

Is Pressure Equipment Directive (2014/68/EU) certifiable?

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Certification depends on the hazard category and conformity module. Higher categories require a Notified Body, while low-risk equipment may follow sound engineering practice or simpler modules.

What should a Pressure Equipment Directive (2014/68/EU) implementation start with?

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Start by defining scope and accountable owners, then map the applicable requirements to existing products, services, systems, suppliers and evidence. A focused gap assessment should identify missing tests, records, procedures, labels, declarations, risk assessments or assurance steps before detailed remediation begins.

What evidence is useful for Pressure Equipment Directive (2014/68/EU)?

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Useful evidence includes classification worksheets, design calculations, material certificates, welding qualifications, pressure-test records, final inspection records, Notified Body certificates, instructions and declarations of conformity. Evidence should be version-controlled, traceable to requirements and owners, retained for the required period and ready for customers, auditors, certification bodies, regulators or market-surveillance authorities.

How often should Pressure Equipment Directive (2014/68/EU) compliance be reviewed?

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Review it on a planned cycle and whenever products, services, suppliers, manufacturing sites, legal requirements, harmonised standards, test methods, incidents, customer commitments or market access assumptions change. High-risk products and regulated services should also be reviewed after complaints, field failures or regulator guidance.

Official Documentation

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Implementation Timeline

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May 2014
Directive 2014/68/EU adopted (recast of 97/23/EC)
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Jul 2016
PED 2014/68/EU became fully applicable
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Ongoing
Harmonised standards (EN 378, EN 13445 series) updated

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