Measuring Equipment (Capacity Measures) Regulations (Northern Ireland) 1998

Construction of capacity measures

6.—(1) Every capacity measure shall be so constructed that—

(a) it does not rock when its base is on a flat, horizontal surface;

(b) its brim and lines are horizontal, when its base is on a flat, horizontal surface;

(c) it remains reasonably perpendicular when rotated about its vertical axis;

(d) air is not trapped on filling; and

(e) liquid or solid is not trapped on emptying when tilted so that its vertical axis is at an angle of 135 degrees from the vertical for any rotational orientation about that axis.

(2) Save where paragraph (4) has effect, dispensing measures for pharmaceutical purposes shall comply with the requirements of BS 604: 1982 or BS 1922: 1987.

(3) In the case of a double measure—

(a) the measure shall be so constructed that it is readily identifiable as a double measure;

(b) the part of the measure having the greater capacity shall have a purported value which is twice that of the part having the lesser capacity; and

(c) neither part of the measure shall be a graduated measure or a subdivided measure.

(4) Any capacity measure, instead of complying with the requirements of paragraph (1) or (2) as the case may be, may comply with—

(a) a relevant national standard or code of practice issued by a national standards body or similar body in a member State or an EEA State;

(b) a relevant international standard officially recognised for use in a member State or an EEA State;

(c) a relevant technical provision of mandatory application in relation to marketing or use in a member State or an EEA State; or

(d) descriptive technical documents relating to manufacturing processes lawfully carried out in a member State or an EEA State, being documents which are sufficiently detailed to enable the measures to be evaluated (if necessary by the carrying out of tests) as capacity measures for use otherwise than as dispensing measures for pharmaceutical purposes or as such dispensing measures, as may be appropriate,

being requirements which, in any case, afford in use at least equivalent standards of safety, suitability and fitness for purpose of such measures as does paragraph (1) and, in the case of dispensing measures for pharmaceutical purposes, BS 604: 1982 or BS 1922: 1987.

(5) In paragraph (4)(d) references to descriptive technical documents are references to such documents which are either published and available to members of the public or are made available by the manufacturer on request—

(a) to any person who is a user or potential user of the capacity measures in question; and

(b) to an inspector for the purposes of the performance by him of his functions under the Order or these Regulations relating to inspection, testing, passing as fit for use for trade and stamping of a capacity measure.