Paragraph 43 Amendment to Schedule 6I1

Schedule 6 is amended as follows.

In the shoulder reference for “Regulation 50” substitute “ Regulation 48 ”.

In the heading for “notified” substitute “ approved ”.

For “a notified body”, in each place it occurs, substitute “ an approved body ”.

For “the notified body”, in each place it occurs, substitute “ the approved body ”.

In paragraph 5—

After paragraph 5 insert—

“5A

(1)

Pyrotechnic articles must be labelled with a UK registration number comprising the following:

(a)

the four-digit identification number of the approved body that has issued a Type-examination certificate (Schedule 2A, Module B), certificate of conformity (Schedule 2A, Module G) or quality system approval (Schedule 2A, Module H), as applicable;

(b)

the category of the pyrotechnic article for which conformity is certified in abbreviated format, in upper case—

(i)

F1, F2, F3 or F4 for fireworks of category 1, 2, 3 and 4 respectively;

(ii)

T1 or T2 for theatrical pyrotechnic articles of category T1 and T2 respectively; and

(iii)

P1 or P2 for other pyrotechnic articles of category P1 and P2 respectively; and

(c)

the processing number used by the approved body for the pyrotechnic article.

(2)

The UK registration number must be structured as follows: ‘XXXX — YY — ZZZZ…’, where XXXX refers to sub-paragraph (1)(a), YY refers to sub-paragraph (1)(b) and ZZZZ… refers to sub-paragraph (1)(c).”

In paragraph 6—

After para 6 insert—

“6A

(1)

Entries made in the register from F2IP completion day must contain at least the following information:

(a)

UK registration number;

(b)

date of issue of Type-examination certificate (where the conformity assessment procedure set out in Part 1 of Schedule 2A (Module B) has been undertaken), certificate of conformity (where the conformity assessment procedure set out in Part 5 of Schedule 2A (Module G) has been undertaken) or quality system approval (where the conformity assessment procedure set out in Part 6 of Schedule 2A (Module H) has been undertaken) as applicable, and date of expiry where applicable;

(c)

manufacturer;

(d)

type of product (generic) and subtype, if applicable;

(e)

where applicable, which conformity assessment procedure has been undertaken from those set out in Part 2 of Schedule 2A (Module C2), Part 3 of Schedule 2A (Module D) and Part 4 of Schedule 2A (Module E); and

(f)

where applicable, the approved body that undertook the conformity assessment procedure described in sub-paragraph (e).

(2)

Sub-paragraphs (1)(e) and (1)(f) apply where the register is maintained by an approved body carrying out the conformity assessment procedure set out in Part 1 of Schedule 2A (Module B), except where the relevant information is not known to that approved body.”.

In paragraph 7, for “harmonised” substitute “ designated ”.

In paragraph 14 for “notified under the Directive” substitute “ approved under these Regulations ”.

In paragraph 15—