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Europe Product Certification

Europe Product Certification


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European Product Certification Introduction

CE PED | Pressure equipment

PED is abbreviation of Pressure Equipment Directive (2014/68/EU), which is a pressure equipment instruction that applies to design, manufacture and conformity assessment of pressure equipment and components with a maximum permissible pressure of 0.5 bar or more. Manufacturers wishing to export their products to EU countries must be certified in accordance with the Pressure Equipment Directive, which was amended from 97/23/EC to 2014/68/EU as of July 19, 2016.

  • Scope

    Scope

    This guidance applies to the design, manufacture and conformity assessment of pressure equipment and assemblies with a maximum permissible pressure of 0.5 bar or more. Includes all vessels, piping, safety accessories and pressure accessories.

      ✤ Applied pressure equipment
    • Water pipe boiler
    • Heat Exchanger
    • Pressure vessel
    • Pipe
    • Electric heater
    • Valve (Isolated, Controlled)
    • Meter
    • Release valve
    • Safety valve
    • Controlled safety pressure release system
    • Pressure switch
    • Temperature change
    • Fluid level switch
      ✤ Excluded scope
    • Items applicable to SPVD(Simple Pressure Vessels Directive) and TPED(Transportable Pressure Equipment Directive)
    • Products with relatively low pressurization : Mechanical Directive
    • Pressure vessel
    • Equipment for vehicles, etc.
  • Proof of pressure equipment (CE marking)

    Proof of pressure equipment (CE marking)

    Pressure instruments are classified into four stages of Category I, II, III, and IV according to the maximum allowable pressure (PS), fluid use, volume, and external diameter (DN), and are subject to the module requirements applicable to that category as shown in the table below. For detailed technical requirements for conformity assessment, European technical specifications such as EN 1345, AD2000, and ASME codes are applied.

    ✤ Annex II, Conformity assessment table

    Category

    Modules

    I

    Module A

    II

    Modules A2, D1, E1

    III

    Modules B(Design type)+D, B(Design type)+F, B(Production type)+E, B(Production type)+C2, H

    IV

    Modules B(Production type)+D, B(Production type)+F, G, H1

    ✤ Annex III, Conformity assessment table

    Module A

    Internal production management

    Module A2

    Internal production management + Product inspection under supervision at random cycles

    Module B

    EU-Type inspection (Production type)
    EU-Type inspection (Design type)

    Module C2

    Formal conformity based on internal production management + Product inspection under supervision at random cycles

    Module D/D1

    D: Formal suitability based on quality assurance of production process
    D1: Quality Assurance of Production Process

    Module E/E1

    E: Formal suitability based on product quality assurance
    E1: Quality Assurance of Inspection and Testing of Final Products

    Module F

    Formal suitability based on product verification

    Module G

    Conformity based on unit verification

    Module H/H1

    H: Conformity based on full quality assurance
    H1: Conformity based on complete quality assurance + Design inspection

  • IGC’s Competency

    IGC’s Competency

    • IGC provides product certification services to companies that want to export their products to Europe based on years of experience.
    • We provide the most competitive product certification service through cooperation with leading overseas product certification institutions.
    • ISO 9000, Companies that already comply quality management systems can make the most of their current quality systems and meet the essential safety requirements of PEDs.
    • If the manufacturer has not been formally certified as a Quality Management System, IGC will provide certification authority services in accordance with the PED QA approach.

Related Services from IGC

  • 01System certification (ISO 13485, ISO 15378, ISO 14155)

  • 02Product certification (European CE certification, clinical evaluation, medical device registration [Eurasia, China, USA, Thailand, Taiwan])

  • 03Certification of Auditor Qualifications

  • 04Professional manpower training and education