Minimise risk and gain a competitive edge
Minimise risk and gain a competitive edge
The European Pressure Equipment Directive (PED) 2014/68/EU provides mandatory requirements for the design, manufacture, and conformity assessment of pressure equipment with a maximum allowable pressure above 0.5 bar (7.25 psig). Compliance with this Directive is essential for designers and manufacturers who intend to place their equipment on the EU market. The PED covers a wide range of pressure equipment, including pressure vessels, piping, pressure accessories, steam boilers, safety accessories, and assemblies.
To achieve compliance with PED 2014/68/EU, pressure equipment must be certified by a Notified Body, which will guide through the accreditation process and help meet production deadlines.
TÜV SÜD Industry Service is an accredited Notified Body for the Pressure Equipment Directive 2014/68/EU, offering comprehensive support to help navigate requirements and smoothly enter the European market.
The conformity assessment procedure provides inspection and quality assessments depending on the environmental impact and level of risk if equipment failure should occur.
The steps include:
| Increase Market Access: Enables expansion into the European market. | |
| Assured Safety and Reliability: Demonstrates product safety and dependability to end users and regulators. | |
| Official Recognition: Confirms conformity with harmonised European standards. | |
| Enhanced Market Competitiveness: Shows commitment to quality and regulatory compliance. |
CE marking shows PED compliance and must be affixed before placing equipment on the EU market.
Documentation includes:
Equipment covered under the Pressure Equipment Directive (PED) includes pressure vessels, pressure accessories, piping, steam boilers, safety accessories, and assemblies that operate above 0.5 bar gauge pressure.
The manufacturer is responsible for PED compliance. They must ensure the equipment meets all essential safety requirements, perform or coordinate conformity assessments, and provide the required technical documentation and CE marking before placing the product on the market.
The timeline varies depending on the complexity of the equipment and the conformity assessment procedure required. Factors such as design documentation, manufacturing stage, and notified body availability can influence the total timeline.
PED certification requires documents such as declaration of conformity, technical documentation and Risk assessment records. These documents verify compliance with pressure, safety, and quality standards set by the directive.
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