5.Design and manufacture in accordance with essential health and safety requirements
8.Retention of technical documentation and EU declaration of conformity
12.Labelling and packaging of products, other than components
15.Duty to take action in respect of a product placed on the market which is considered not to be in conformity
18.Prohibition on placing on the market products which are not in conformity
19.Requirements which shall be satisfied before an importer places a product on the market
20.Prohibition on placing on the market products considered not to be in conformity with the essential health and safety requirements
25.Duty to take action in respect of a product placed on the market which is considered not to be in conformity
27.Retention of technical documentation and EU declaration of conformity
29.Requirements which shall be satisfied before a distributor makes a product available on the market
31.Prohibition on making available on the market where product not considered to be in conformity with safety objectives
32.Duty to take action in respect of products made available on the market which are not in conformity
ESSENTIAL HEALTH AND SAFETY REQUIREMENTS
COMMON REQUIREMENTS FOR EQUIPMENT AND PROTECTIVE SYSTEMS
1.A conformity assessment body shall be established in Northern Ireland...
2.A conformity assessment body shall be a third party body...
3.A body belonging to a business association or professional federation...
4.(1) A conformity assessment body, its top level management and...
5.A conformity assessment body, its top level management and the...
6.A conformity assessment body, its top level management and the...
7.A conformity assessment body shall ensure that the activities of...
8.A conformity assessment body and its personnel shall carry out...
9.A conformity assessment body shall be capable of carrying out...
10.A conformity assessment body shall have— (a) personnel with technical...
11.A conformity assessment body shall have the means necessary to...
12.The personnel responsible for carrying out conformity assessment activities shall...
13.A conformity assessment body shall be able to demonstrate the...
14.The remuneration of the top level management and the personnel...
15.A conformity assessment body shall have, and shall satisfy the...
16.A conformity assessment body shall ensure that its personnel observe...
17.Paragraph 16 does not prevent the personnel from providing information...
18.A conformity assessment body shall participate in, or ensure that...
OPERATIONAL OBLIGATIONS OF NOTIFIED BODIES
1.A notified body shall carry out conformity assessments in accordance...
2.A notified body shall carry out conformity assessments in a...
3.A notified body shall perform its activities taking due account...
5.Where a notified body finds that essential health and safety...
6.Where, in the course of the monitoring of conformity following...
7.Where the notified body has required a manufacturer to take...
8.Paragraph 9 applies where a notified body is minded to—...
11.A notified body shall make provision in its contracts with...
12.A notified body shall provide other bodies notified under the...
14.A notified body shall— (a) acknowledge receipt of the technical...
ENFORCEMENT POWERS OF THE HEALTH AND SAFETY EXECUTIVE FOR NORTHERN IRELAND UNDER THE 1978 ORDER
EU DECLARATION OF CONFORMITY (No. XXXX)
1.Product model/product (product, type, batch or serial number):
2.Name and address of manufacturer and, where applicable, the authorised...
3.This declaration of conformity is issued under the sole responsibility...
4.Object of the declaration (identification of product allowing traceability; it...
5.The object of the declaration described above is in conformity...
6.References to the relevant harmonised standards used or references to...
7.Where applicable, the notified body (name, number) performed (description of...
8.Additional information: Signed for and on behalf of: (place and...