- Latest available (Revised)
- Point in Time (08/12/2016)
- Original (As made)
There are currently no known outstanding effects for the The Simple Pressure Vessels (Safety) Regulations 2016.
Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.
PART 2 Obligations of economic operators
4.Design and manufacture in accordance with essential safety requirements and sound engineering practice
5.Technical documentation and conformity assessment for category A vessels
6.EU declaration of conformity, CE marking and inscriptions for category A vessels
8.Retention by manufacturer of technical documentation and EU declaration of conformity
13.Duty of manufacturer to take action in respect of vessels placed on the market which are considered not to be in conformity
17.Prohibition on placing on the market vessels which are not in conformity
18.Requirements which must be satisfied before an importer places a category A vessel on the market
19.Prohibition on an importer placing on the market a category A vessel considered not to be in conformity with the essential safety requirements
20.Requirements which must be satisfied before an importer places a category B vessel on the market
24.Monitoring by importer of vessels made available on the market
25.Duty of importer to take action in respect of vessels placed on the market which are considered not to be in conformity
26.Retention by importer of technical documentation and EU declaration of conformity
29.Requirements which must be satisfied before a distributor makes available on the market a category A vessel
30.Prohibition on a distributor making available on the market a category A vessel not considered to be in conformity with essential safety requirements
31.Requirements which must be satisfied before a distributor makes a category B vessel available on the market
33.Duty for distributor to take action in respect of vessels made available on the market which are not in conformity
Conformity Assessment Procedures
PART 1 EU-Type Examination (Module B)
1.EU-type examination (Module B) is a conformity assessment procedure in...
2.(1) A manufacturer must lodge an application for EU-type examination...
3.(1) The technical documentation referred to in paragraph 2(2)(c) must—...
4.(1) The notified body must examine the technical documentation and...
5.The notified body must draw up an evaluation report that...
6.(1) Where the type meets the requirements of these Regulations,...
8.(1) Each notified body must inform the Secretary of State...
9.A manufacturer must keep a copy of the EU-type examination...
PART 4 Conformity to type based on internal production control (Module C)
2.Name and address of the manufacturer and, where applicable, his...
3.This declaration of conformity is issued under the sole responsibility...
4.Object of the declaration (identification of the vessel allowing traceability;...
5.The object of the declaration described above is in conformity...
6.References to the relevant harmonised standards used or references to...
7.The notified body (name, number) performed (description of intervention) and issued the...
8.Additional information: Signed for and on behalf of: (place and...
PART 1 Notified Body Requirements
1.A conformity assessment body must be established in the United...
2.A conformity assessment body must be a third party body...
3.(1) A conformity assessment body, its top level management and...
4.A conformity assessment body, its top level management and the...
5.A conformity assessment body must ensure that the activities of...
6.A conformity assessment body and its personnel must carry out...
7.A conformity assessment body must be capable of carrying out...
9.A conformity assessment body must have the means necessary to...
10.The personnel responsible for carrying out conformity assessment must have—...
11.A conformity assessment body must be able to demonstrate the...
12.The remuneration of the top level management and the personnel...
13.A conformity assessment body must have, and must satisfy the...
14.A conformity assessment body must ensure that its personnel observe...
15.Paragraph 14 does not prevent the personnel from providing the...
16.A conformity assessment body must participate in, or ensure that...
PART 2 Operational obligations of notified bodies
17.A notified body must carry out conformity assessments in accordance...
18.A notified body must carry out conformity assessments in a...
19.A notified body must perform its activities taking due account...
21.Where a notified body finds that essential safety requirements or...
22.Where, in the course of the monitoring of conformity following...
23.Where the notified body has required a manufacturer to take...
24.Paragraph 25 applies where a notified body is minded to—...
26.A notified body must inform the Secretary of State of—...
27.A notified body must make provision in its contracts with...
28.A notified body must provide other bodies notified under these...
Enforcement powers of the Health and Safety Executive for Northern Ireland under the 1978 Order
Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.
Original (As Enacted or Made): The original version of the legislation as it stood when it was enacted or made. No changes have been applied to the text.
Point in Time: This becomes available after navigating to view revised legislation as it stood at a certain point in time via Advanced Features > Show Timeline of Changes or via a point in time advanced search.
Explanatory Memorandum sets out a brief statement of the purpose of a Statutory Instrument and provides information about its policy objective and policy implications. They aim to make the Statutory Instrument accessible to readers who are not legally qualified and accompany any Statutory Instrument or Draft Statutory Instrument laid before Parliament from June 2004 onwards.
Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:
Impact Assessments generally accompany all UK Government interventions of a regulatory nature that affect the private sector, civil society organisations and public services. They apply regardless of whether the regulation originates from a domestic or international source and can accompany primary (Acts etc) and secondary legislation (SIs). An Impact Assessment allows those with an interest in the policy area to understand:
This timeline shows the different points in time where a change occurred. The dates will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. The first date in the timeline will usually be the earliest date when the provision came into force. In some cases the first date is 01/02/1991 (or for Northern Ireland legislation 01/01/2006). This date is our basedate. No versions before this date are available. For further information see the Editorial Practice Guide and Glossary under Help.
Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:
Click 'View More' or select 'More Resources' tab for additional information including:
The data on this page is available in the alternative data formats listed: