The Directive defines a number of classifications for pressure equipment, based on their hazard level which is determined based on stored energy (pressure-volume product) and the nature of the contained fluid. Assessment and conformity procedures are different for each category, ranging from self-certification for the lowest (category I) hazard up to full ISO9001 quality management and/or notified body type examination for category IV equipment. Aspects of the design, production and testing of the equipment are the subject of a large number of harmonized standards to aid compliance with the essential requirements of the directive.
Manufacturers must also provide adequate instructions with equipment, complete a specified declaration of conformity and maintain a technical file of information about how the equipment was designed and manufactured. Pressure equipment must be marked with the manufacturer, unique identification of model and serial number, the year of manufacture, maximum/minimum allowable pressure limits and the CE logo |
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