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The Medical Devices (Northern Ireland Protocol) Regulations 2021

Status:

This is the original version (as it was originally made).

Regulation 23

SCHEDULE 3Provisions breach of which is an offence under regulation 23

This schedule has no associated Explanatory Memorandum

Table 1

RegulationTitle of the regulation
5Reprocessing of single-use devices
6Requirement on health institutions relating to implanted devices
7Provision of information relating to custom-made devices
9Retention of documentation relating to conformity assessments and custom-made devices
10UK(NI) indication
11Ethical review of clinical investigations
12(1)Prior authorisation of clinical investigations by the Secretary of State
14Damage compensation in relation to clinical investigations
15Retention of documentation relating to clinical investigations

Table 2

ArticleTitle of the article
5(1) to (3), (5)Placing on the market and putting into service
6(1)-(3)Distance sales
7Claims
9(3), (4)Common specifications
10 (except in paragraph 14, only the first sub-paragraph)General obligations on manufacturers
11(1), (3), (6)Authorised representative
12Change of authorised representative
13General obligations of importers
14General obligations of distributors
15Person responsible for regulatory compliance
16(3), (4)Cases in which obligations of manufacturers apply to importers, distributors or other persons.
17(1)Single-use devices and their reprocessing
18(1)Implant card and information to be supplied to the patient with an implanted device
21(2)Devices for special purposes
22(1), (3) to (5)Systems and procedure packs
23(1)Parts and components
25(1), (2)Identification within the supply chain
32(1), (2)Summary of safety and clinical performance
52(1) to (4), (6) to (11), (13)Conformity assessment procedures
53(3)Involvement of notified bodies in conformity assessment procedures
58(1)Voluntary change of notified body
62(1), (2) (only the first sub-paragraph), (3) (only the first sub-paragraph), (4), (5), (7)General requirements regarding clinical investigations conducted to demonstrate conformity of devices
82(1)Requirements regarding other clinical investigations
84Post-market surveillance plan
85Post-market surveillance report
86Periodic safety update report
89(1), (3) (only the second sub-paragraph),(5), (8)Analysis of serious incidents and field safety corrective actions
94 (only the final paragraph)Evaluation of devices suspected of presenting an unacceptable risk or other non-compliance

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