Regulation 4 Amendment to the Consumer Rights Act 2015

In the Consumer Rights Act 2015^f1, Schedule 5^f2 (investigatory powers etc.) is amended as follows—

(a)

in paragraph 8, after the definition of “Regulation (EU) 2017/745 on medical devices” insert—

““Regulation (EU) 2017/746 on in vitro diagnostic medical devices” means Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU;”;

(b)

in paragraph 19(7A)(a)—

(i)

at the end of sub-paragraph (iii), omit “or”;

(ii)

at the end of sub-paragraph (iv), omit “and” and insert—

“or

(v)

Regulation (EU) 2017/746 on in vitro diagnostic medical devices, and”;

(c)

in paragraph 30A(3)(b), after “Regulation (EU) 2017/745 on medical devices” insert “or Regulation (EU) 2017/746 on in vitro diagnostic medical devices”.

Annotations

Footnotes

f1: 2015 c. 15.
f2: Schedule 5 was amended by the Medicines and Medical Devices Act 2021, S.I. 2021/858 and S.I. 2021/905; there are other amending instruments but none is relevant.