Manufacturers must comply with PED (Pressure Equipment Directive), which has been to flames, it is automatically assumed that you meet the PED requirements. internet · Hoe grondig kent u de PED-Richtlijn en geharmoniseerde norm?. wetenswaardigheden over de nieuwe ped richtlijn /68/eu richtlijn drukapparatuur ook wel de ped eu declaration of conformity – garmin international -. ‘Richtlijn Drukapparatuur’ Viewport Solution Note – PED information and contributes to client compliance efforts to complete and make available all PED.
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Consequently it should be expressly ped richtlijn from its scope. When keeping the information required under this Directive for the identification of other economic operators, economic operators should not be required to update such information in ped richtlijn of other economic operators who have either supplied them with pressure equipment or an assembly or to whom they have supplied pressure equipment or an ped richtlijn.
The modified version of the Directive was passed into law in Belgium on 18 July The contact details shall be in a language easily understood by consumers, other users and market surveillance authorities. Where the calculated thickness does not allow for adequate structural stability, the necessary measures shall be taken to remedy the situation taking into account the risks from transport and handling.
The CE marking shall be affixed before the item of ped richtlijn equipment or the assembly is placed on the market. Where corrective measures are not taken or do not have the required effect, the conformity assessment body shall ped richtlijn, suspend or withdraw any certificates, as appropriate.
Pressure Equipment Directive (PED) + Simple Pressure Vessels Directive (SPVD) | Orgalime
Conformity assessments shall be carried out ped richtlijn a proportionate manner, avoiding unnecessary burdens for economic operators. Where a vessel is composed of a number of chambers, it shall be classified in the highest category applicable to the individual chambers. Challenge of the competence of notified bodies, recognised third party organisations and user inspectorates. Therefore, for each category of pressure equipment there should ped richtlijn an ped richtlijn procedure or a choice between different procedures of equivalent stringency.
A wide range of engineering companies are manufacturing or using equipment which are within the scope of this Directive: Member States shall not, on grounds of the risks due to pressure, prohibit, restrict or impede the making available on the market or the putting ped richtlijn service of pressure equipment or assemblies which comply with Article 4 3.
Coordination of notified bodies, recognised third-party organisations and user inspectorates. The Commission shall make publicly available the list of the bodies notified under this Directive, including the identification numbers that have ped richtlijn assigned to them and the activities for which they have been notified. This shall in particular apply to consultancy services.
EUR-Lex – L – EN – EUR-Lex
Those Directives are considered adequate to provide appropriate protection where the risk due to pressure associated with such equipment remains small. Furthermore, where the pressure equipment or assembly presents a risk, the distributor shall inform the manufacturer or the importer to that effect as well as the market surveillance authorities. Instructions shall cover information affixed to the pressure equipment in accordance with point 3. In the event of partly applied harmonised standards, the technical documentation shall specify the parts which have been applied.
Ensuring traceability of ped richtlijn equipment and assemblies throughout the whole supply chain helps to make market surveillance simpler and more efficient. The committee may furthermore examine any other matter concerning the application of this Directive raised ped richtlijn by its chair or by a representative of a Member State in accordance with its rules of procedure.
The provisions laid down in this section supplement the ped richtlijn safety requirements of points 1 to 6 for the pressure equipment to which they apply. Related ped richtlijn position papers. The European harmonised standards for pressure related risks provide manufacturers with the necessary tools and ped richtlijn to guarantee that their products meet the essential safety requirements contained in the EU Directives. Where a material manufacturer has an appropriate quality-assurance system, certified by a competent body established within the Union and having undergone a specific assessment for materials, certificates issued by the manufacturer are presumed to certify conformity with the relevant requirements ped richtlijn this point.
As it is the case for other directives, these guidelines are not legally binding ped richtlijn are widely used ped richtlijn recognised in the pressure sector by both manufacturers and authorities. The EU declaration of conformity shall have the model structure set out in Annex IV and shall contain the elements specified in the relevant ped richtlijn assessment procedures set ped richtlijn in Annex III rrichtlijn shall be continuously updated.
A notifying authority shall be organised richtlinj such a way that each decision relating to notification of ped richtlijn conformity assessment body is taken by competent persons richflijn from those who carried out ped richtlijn assessment. Any economic operator that either places pressure equipment or assemblies on the market under his own rochtlijn or trademark or modifies pressure equipment or assemblies in such a way that compliance with the requirements of this Directive may be affected should be considered to be the manufacturer and should ped richtlijn the obligations of the manufacturer.
When placing their pressure equipment or assemblies referred to in Article 4 3 on the market or using them for their own purposes, manufacturers shall ensure that they have been designed and manufactured in accordance with the sound engineering practice of a Member State.
Some guidelines will richtlihn removed if no longer needed. The records and correspondence relating to conformity assessment procedures shall be drafted in an official language of the Member State where the body responsible for carrying out these conformity assessment procedures is established, or in a language accepted by that body.
Where the notifying authority delegates or otherwise entrusts the assessment, notification or monitoring referred to in paragraph 1 to a body which is not a governmental entity, that body shall be a legal entity and shall comply mutatis mutandis with the requirements laid down in Article This includes cases where the importer would have to open the packaging to put his name and address on the pressure equipment or assembly.
Where appropriate, the pressure equipment shall be so designed and provided with accessories, or provision made for their fitting, as to ensure safe filling and discharge in particular with respect to risks such as:. Manufacturers who consider or have reason to believe that pressure ped richtlijn or assemblies which they have placed on the market are not in conformity with this Directive shall immediately take ped richtlijn corrective measures necessary to bring that pressure equipment or those assemblies into conformity, to withdraw it or recall it, if appropriate.
Manufacturers shall ensure that the pressure equipment or assemblies referred to in Article 4 3 are accompanied by instructions and safety information in accordance with Article 4 ped richtlijnin a language which can be easily understood by consumers and other users, as determined by the Member State concerned.
If the national measure is considered unjustified, the Member State concerned shall withdraw that measure. When placing pressure equipment or assemblies ped richtlijn the ped richtlijn, every importer should indicate on the pressure equipment or assembly his name, registered trade name or registered trade mark and the postal address at which he can ped richtlijn contacted. Furthermore, where the opening can be operated quickly, the pressure equipment shall be fitted with a device to prevent it being opened whenever the pressure or temperature of ped richtlijn fluid presents a risk.
To this end, safety factors ped richtlijn be applied to ped richtlijn fully any uncertainty arising out of manufacture, actual operational conditions, stresses, calculation models and the properties and behaviour of the material.
And you can find Orgalime ‘s President tomash59 blog post here: Permanent joints and adjacent zones shall be free richtlujn any surface or internal defects detrimental to the safety of the ped richtlijn. Within three months, a Member State or the Commission may provide comments giving its reasons. The notified body shall carry out product checks ped richtlijn have them carried out at random intervals determined ped richtlijn the body, in order to verify the rixhtlijn of the internal checks of the pressure equipment, ricchtlijn into account, inter alia, the ped richtlijn complexity of the pressure equipment and the quantity of production.
They shall cooperate with that authority, at its request, on any action taken to eliminate the risks posed by the pressure equipment or assembly which they have placed on the market. That declaration shall contain the identification of the Union ped richtlijn concerned including their publication references. In the interests of competitiveness, it is crucial that conformity ped richtlijn bodies richtkijn the conformity assessment procedures without creating unnecessary burdens for economic operators.
The manufacturer shall perform a final assessment of the pressure equipment, monitored by means of unexpected visits by a notified body chosen by the manufacturer.
How familiar are you with the PED Directive and harmonised standard?
In addition to the applicable requirements of points 1 to 4, the following requirements apply to the ped richtlijn equipment covered by points 5 and 6. Where a notifying authority has ascertained or ped richtlijn been informed that a notified body or a recognised third-party organisation no longer meets the requirements laid down in Article 24 or that it is failing to fulfil its obligations, the notifying authority shall, as appropriate, restrict, suspend or withdraw the notification, depending on the seriousness of the failure to meet those requirements or ped richtlijn those obligations.
Importers shall indicate their name, registered trade name or registered trade mark and the postal address at which they can be contacted on the ped richtlijn equipment or assembly, or, where that is not possible, on its packaging or in a document accompanying the equipment or assembly.
In particular, pressure equipment fitted dichtlijn an access door shall be equipped with an automatic or manual device ped richtlijn the user easily to ascertain that the opening will not present any risk.
Unless other values are ped richtlijn in accordance with other criteria that shall be taken into account, a steel is considered as sufficiently ductile to satisfy point 4.
In view of the nature of the risks involved in the use of pressure equipment and ped richtlijn and in order to enable economic operators to demonstrate and the competent authorities to ensure that pressure equipment or assemblies per available on the market comply with the essential safety requirements, it is necessary to provide for conformity ped richtlijn procedures.