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The Pressure Equipment (Safety) Regulations 2016
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Changes over time for: Section 43
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43.—(1) The [F1approved] body or user inspectorate must, when performing unexpected visits in the framework of quality assurance procedures for pressure equipment in categories III and IV in regulation 6(a)(i), 6(a)(ii)(aa) or 6(b), take a sample of equipment from the manufacturing or storage premises in order to perform, or have performed, the final assessment as referred to in paragraph 25 of Schedule 2.
(2) The manufacturer must inform the [F1approved] body or user inspectorate of the intended schedule of production.
(3) The [F1approved] body or user inspectorate must carry out at least two visits during the first year of manufacturing.
(4) The [F1approved] body or user inspectorate must determine the frequency of subsequent visits on the basis of the criteria set out in point 4.4. of modules D, E and H and point 5.4 of module H1 in [F2Schedule 1A to these Regulations].
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E1This version of this provision extends to England and Wales and Scotland only; a separate version has been created for Northern Ireland only
Textual Amendments
F1Word in reg. 43(1)-(4) substituted (E.W.S.) (22.4.2024) by The Pressure Equipment (Safety) (Amendment) Regulations 2024 (S.I. 2024/490), regs. 1(2), 2(3)
F2Words in reg. 43(4) substituted (E.W.S.) (31.12.2020) by The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 24 para. 29 (with Sch. 24 para. 41) (as amended by S.I. 2020/676, regs. 1(1), 2); 2020 c. 1, Sch. 5 para. 1(1)
43.—(1) The notified body or user inspectorate must, when performing unexpected visits in the framework of quality assurance procedures for pressure equipment in categories III and IV in regulation 6(a)(i), 6(a)(ii)(aa) or 6(b), take a sample of equipment from the manufacturing or storage premises in order to perform, or have performed, the final assessment as referred to in paragraph 25 of Schedule 2.
(2) The manufacturer must inform the notified body or user inspectorate of the intended schedule of production.
(3) The notified body or user inspectorate must carry out at least two visits during the first year of manufacturing.
(4) The notified body or user inspectorate must determine the frequency of subsequent visits on the basis of the criteria set out in point 4.4. of modules D, E and H and point 5.4 of module H1 in Annex III to the Directive (as amended from time to time).
Extent Information
E2This version of this provision extends to Northern Ireland only; a separate version has been created for England and Wales and Scotland only
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