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Ensure CE Compliance for Pressure Equipment with Kiwa

If you manufacture pressure equipment for the European market, compliance with the Pressure Equipment Directive (PED) 2014/68/EU is mandatory. This EU directive requires that all pressure equipment operating above 0.5 bar is CE marked—proving it meets essential safety requirements and can be legally sold across the European Economic Area (EEA).
As an independent Notified Body, Kiwa offers complete conformity assessment and certification services under PED 2014/68/EU. We support manufacturers throughout the certification process to ensure equipment meets the applicable design, manufacturing, and testing standards.

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Why pressure equipment certification matters

Pressure equipment that is not properly designed or manufactured can pose serious risks to people, property, and the environment. The PED provides a strict regulatory framework to minimize these risks and to ensure that only safe, compliant products reach the market.

Kiwa’s PED certification services help you demonstrate that your products:

  • Comply with EU safety regulations
  • Meet technical and performance standards
  • Are safe to use and built to last
  • Can be legally traded within the EU with the CE mark

Product certification and CE marking

We provide product certification and approval for a wide range of pressure equipment. Our experts review technical documentation (such as design drawings and material specifications), inspect manufacturing processes, and conduct or witness required testing. Once conformity is confirmed, you gain the right to affix the CE marking to your product. This is a legal requirement for selling pressure equipment within the European Economic Area.

Examples of pressure equipment Kiwa certifies

  • Pressure vessels
  • Heat exchangers
  • Steam generators
  • Boilers
  • Autoclaves
  • Pressure accessories (e.g., safety valves, gauges)
  • Piping systems
  • Assemblies with multiple pressure components

Module B – EU Type Examination

EU type examination is an option for high-risk categories. With a type certificate, the design can be a required step. This module involves an assessment of a representative design or prototype by Kiwa. If compliant, we issue an EU Type Examination Certificate. This certificate forms the basis for production and additional modules.

Quality System Certification

In addition to product certification, we offer Quality System Certification under PED. This method shifts the focus from inspecting individual products to evaluating the manufacturer’s entire quality management system.

Benefits of PED quality system certification:

  • CE marking based on internal production controls
  • Reduced need for repeated inspections
  • Ideal for serial production or batch manufacturing
  • Includes regular audits and surveillance by Kiwa

Benefits of working with Kiwa

Independent Notified Body

Independent, recognized Notified Body under PED 2014/68/EU

Comprehensive certification support

Comprehensive guidance and support throughout the certification process

Streamlined tailored procedures

Streamlined procedures tailored to your production model

Enhanced trust

Enhanced trust and credibility for your brand and products

Clear communication

Fast, clear communication from experienced professionals

Frequently Asked Questions

What is a Notified Body?

A Notified Body is an organization appointed by an EU country to help make sure certain products meet the right requirement before they can be sold. These organizations play an important role in checking that products follow EU rules by carrying out tasks like testing, inspecting, and certifying them.

What is the Pressure Equipment Directive (PED)?

The PED 2014/68/EU is a European product safety directive that sets technical requirements for pressure equipment operating above 0.5 bar. It ensures products are safe for use and legally marketable in the EU through CE marking.

Which products fall under PED certification requirements?

Products like pressure vessels, boilers, heat exchangers, steam generators, autoclaves, safety accessories (valves, gauges), piping, and assemblies are commonly subject to PED requirements.

What is CE marking and why is it important?

CE marking is a legal requirement in the EU for pressure equipment above 0.5 bar. It shows that your product complies with the essential safety requirements of the PED and allows it to be sold across the European Economic Area.

What is Module B in the PED certification process?

Module B is the EU Type Examination process. It involves evaluating a prototype or design of the pressure equipment to confirm it meets PED safety standards.

Can Kiwa certify our internal quality system under PED?

Yes. Through Modules D, E, or H, we can certify your quality management system. This allows you to CE mark your products based on internal production controls, streamlining the process and saving time.

How long does the PED certification process take?

The duration depends on the complexity of the equipment, the conformity assessment module chosen, and the quality of your documentation. Kiwa ensures efficient processing and transparent timelines.

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