Pressure Equipment Directive PED 2014/68/UE
Directive 2014/68/EU (PED): regulatory framework for pressure equipment | BOIXAC Technical blog › Regulations & certification Directive 2014/68/EU (PED):the regulatory framework for pressure equipment in the EU A technical guide to the scope of application, risk category classification and conformity assessment modules established by the Pressure Equipment Directive. BOIXAC Tech SL Updated: 2026 Reading time: ~8 min Note on the scope of this article This text is exclusively informational and educational in nature. It does not constitute legal, technical or engineering advice, and cannot under any circumstances replace the specific analysis carried out by a qualified professional on a particular piece of equipment. The correct application of Directive 2014/68/EU — including equipment classification, determination of the assessment module and obtaining CE marking — always requires the involvement of competent engineers and, for higher categories, a duly notified Notified Body. BOIXAC assumes no liability arising from decisions made based on the content of this article. Directive 2014/68/EU of the European Parliament and of the Council, of 15 May 2014, on the harmonisation of the laws of Member States relating to the making available on the market of pressure equipment — commonly known as the Pressure Equipment Directive or PED — is the European regulatory instrument governing the design, manufacture and conformity assessment of pressure equipment intended for the internal market. For any manufacturer or industrial user of pressure equipment — heat exchangers, vessels, boilers, process pipework and fittings — understanding the scope and logic of this Directive is a prerequisite for operating safely and in legal compliance within the European Economic Area. 1. Background and regulatory context Directive 2014/68/EU repealed and recast the previous Directive 97/23/EC, which ceased to apply on 19 July 2016. The recast did not substantially modify the essential safety requirements or the conformity assessment tables, but aligned the legislation with the New Legislative Framework (NLF) of the European Union — in particular Regulation (EU) No 765/2008 and Decision 768/2008 — introducing explicit obligations for all economic operators in the supply chain: manufacturers, authorised representatives, importers and distributors. Key regulatory reference Directive 2014/68/EU of the European Parliament and of the Council, of 15 May 2014 (OJ L 189, 27 June 2014, pp. 164–259). Full entry into force: 19 July 2016. 2. Scope of application The Directive applies to the design, manufacture and conformity assessment of pressure equipment and assemblies with a maximum allowable pressure (PS) greater than 0.5 bar gauge. Element Description under the Directive Vessels Housings designed and built to contain fluids under pressure, including shell-and-tube heat exchangers. Piping Piping components intended for the transport of fluids, including pipes, piping systems, fittings, expansion joints and hoses. Safety accessories Devices protecting against the exceedance of allowable limits: safety valves, pressure relief devices, automatic control systems, etc. Pressure accessories Devices with an operational function subject to pressure: non-return valves, regulators, steam traps, filters, etc. Assemblies Several items of pressure equipment assembled by a manufacturer to constitute an integrated functional installation. Notable exclusions The Directive expressly excludes from its scope, among others: simple pressure vessels covered by Directive 2014/29/EU; aerosol generators; equipment intended for vehicle operation; certain water distribution networks; nuclear equipment; and well-control equipment for the extractive industry. 3. Fluid classification and its significance One of the Directive’s central pillars is the classification of the fluids contained in the equipment, which determines — together with the pressure and volume or nominal diameter parameters — the applicable risk category. Directive 2014/68/EU updated the classification relative to the previous legislation, aligning it with Regulation (EC) No 1272/2008 (CLP) on classification, labelling and packaging of substances and mixtures. Group Fluids included (simplified criterion) Group 1 Fluids considered hazardous: explosive, extremely or highly flammable, toxic, very toxic, oxidising and corrosive under the CLP Regulation, as well as any fluid at a maximum allowable temperature (TS) above its flash point. Group 2 All fluids not included in Group 1, commonly referred to as “non-hazardous fluids”. Key technical consideration The Directive establishes that thermal oils are classified as Group 1 when the maximum allowable temperature of the equipment exceeds the flash point of the oil in question, regardless of its CLP classification. This specific criterion, set out in Commission Guideline B-41, has direct implications for the resulting category of the equipment. 4. Risk categories The Directive establishes four risk categories (I to IV) for pressure equipment. Category assignment is determined using the tables in Annex II, which cross-reference fluid parameters with equipment parameters (PS, volume V or nominal diameter DN). Category IMinimal risk Low-pressure or small-volume equipment. The manufacturer may self-certify via Module A (internal production control). Category IILow risk Requires involvement of a Notified Body in the production phase. Available modules: A2, D1, E1. Category IIIModerate risk Notified Body involvement in design and/or production. Modules: B+D, B+F, B+E, B1+D, G, H. Category IVHigh risk Maximum requirements. Notified Body required at all stages. Permitted modules: B+D, B+F, G, H1. 5. Conformity assessment modules Module Name NB required Summary A Internal production control No Manufacturer’s self-declaration. Applicable to Category I only. A2 Internal production control with supervised checks Yes The NB performs random inspections of the finished product. B EU-type examination (production type) Yes The NB examines a representative specimen. Must be combined with a production-phase module (D, E or F). B1 EU-type examination (design type) Yes The NB examines the design technical documentation without a physical prototype. D / D1 Production quality assurance Yes The NB approves and supervises the manufacturer’s quality system in the production phase. E / E1 Product quality assurance Yes The NB approves and supervises the quality system for final inspections and testing. F Product verification Yes The NB verifies each produced unit by examination and testing. G Unit verification Yes Individual assessment of each item by the NB, both in design and production. Common for one-off equipment. H / H1 Full quality assurance Yes The NB approves and supervises the complete quality management system. H1 adds design examination and special surveillance. 6. Economic operator obligations Manufacturer Ensure the equipment … Read more