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Category: Assessment Procedures

PED

Module G does require that a notified body must examine the design of the pressure equipment and it is considered reasonable to expect the notified body to inform the manufacturer of the results of the examination. Module G does not …

PED

The manufacturer himself ensures the conformity of the products to the legislative requirements (no EU-type examination). No notified body is involved for this module. This module is suitable for pressure … more

PED

PED Module A2 product checks at random intervals carried out by a notified body or in-house accredited body. This module is suitable for pressure equipments categories I, and II. Module A2 … more

PED

The manufacturer operates a production (manufacturing part and inspection of final product) quality assurance system in order to ensure conformity to PED requirements. The notified body assesses the production (manufacturing … more

PED

The manufacturer operates a product quality (= production quality without the manufacturing part) assurance system for final product inspection and testing in order to ensure conformity to the PED requirements. The … more

A notified body is an organisation designated by an EU country to assess the conformity of certain products before being placed on the market. These bodies carry out tasks related to conformity assessment procedures set out in the applicable legislation …

PED

Module B is always followed by other modules by which the conformity of the pressure equipment to the approved EU-type is demonstrated. A notified body examines specimen of a type … more

PED

Module B (production) is always followed by other modules by which the conformity of the pressure equipment to the approved EU-type is demonstrated. A notified body examines specimen of a … more

PED

Module B (design) is always followed by other modules by which the conformity of the pressure equipment to the approved EU-type is demonstrated. A notified body examines design of a … more

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