Regulation 7

SCHEDULE 1E+W

ExemptionsE+W

1.—(1) The kinds of single use carrier bags to which regulation 6 does not apply are—

[F1(za)bags used solely to contain one or more items of the following kinds—

(i)unpackaged food for human or animal consumption;

(ii)unpackaged loose seeds, bulbs, corms or rhizomes;

(iii)any unpackaged axe, knife, knife blade or razor blade;

(iv)unpackaged goods contaminated by soil;

(v)items from the categories specified in sub-paragraph (2);]

F2(a). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

F2(b). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

F2(c). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

F2(d). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(e)bags used solely to contain packaged—

(i)uncooked fish or fish products;

(ii)uncooked meat or meat products;

(iii)uncooked poultry or poultry products,

and in respect of which the maximum dimensions are 205 millimetres (“mm”) (width) x 125 mm (gusset width) x 458 mm (height inclusive of handles);

F2(f). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(g)bags used to contain purchases made on board ships, trains, aircraft, coaches or buses;

(h)bags used to contain purchases made in an area designated by the Secretary of State as a security restricted area under section 11A of the Aviation Security Act 1982 M1;

[F3(i)mail order dispatch and courier bags;]

(j)bags which—

(i)are made wholly from paper;

(ii)have maximum dimensions of 175 mm (width) x 260 mm (height);

(iii)do not have a gusset; and

(iv)do not have a handle;

(k)bags which—

(i)are made wholly or mainly from plastic;

(ii)have maximum dimensions of 125 mm (width) x 125 mm (height);

(iii)do not have a gusset; and

(iv)do not have a handle;

(l)bags which—

(i)are made wholly from paper;

(ii)have maximum dimensions of 80 mm (width) x 50 mm (gusset width) x 155 mm (height); and

(iii)do not have a handle;

(m)gusseted liners used to line or cover boxes, crates or other containers of a similar nature;

(n)bags used solely to contain live aquatic creatures in water;

F4(o). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(2) The specified categories are—

(a)medicinal products or listed appliances sold in accordance with a prescription issued by a registered medical practitioner, a dentist, a supplementary prescriber, a nurse independent prescriber, an independent nurse prescriber, an optometrist independent prescriber, a pharmacist independent prescriber or an EEA health professional;

(b)where sold F5...otherwise than in accordance with paragraph (a), pharmacy medicine.

(3) In this paragraph—

M2“dentist” (“deintydd”) means a person registered in the dentists register kept under section 14 of the Dentists Act 1984 ;

M3“EEA health professional” (“proffesiynolyn iechyd yr AEE”) has the meaning given in regulation [F6213(1) of the Human Medicines Regulations 2012];

M4“independent nurse prescriber” (“nyrs sy'n rhagnodi'n annibynnol”) has the meaning given in regulation 2(1) of the [F7National Health Service (Pharmaceutical Services) (Wales) Regulations 2013];

“listed appliances” (“cyfarpar rhestredig”) means listed appliances within the meaning of any of the following—

(a)

M5section 80 of the National Health Service (Wales) Act 2006 ;

(b)

M6article 63 of the Health and Personal Social Services (Northern Ireland) Order 1972 ;

(c)

M7section 27 of the National Health Service (Scotland) Act 1978 ;

(d)

M8section 126 of the National Health Service Act 2006 ;

M9“medicinal product” (“cynnyrch meddyginiaethol”) has the meaning given in section 130 of the Medicines Act 1968;

“pharmacy medicine” (“meddyginiaeth fferyllol”) [F8has the meaning given in regulation 5(5) of the Human Medicines Regulations 2012;]

“prescription only medicine” (“meddyginiaeth drwy bresgripsiwn yn unig”) [F9has the meaning given in regulation 5(3) of the Human Medicines Regulations 2012;]

M10“supplementary prescriber” (“rhagnodydd atodol”), “nurse independent prescriber” (“nyrs-ragnodydd annibynnol”), “optometrist independent prescriber” (“optometrydd-ragnodydd annibynnol”) and “pharmacist independent prescriber” (“fferyllydd-ragnodydd annibynnol”) each have the meanings respectively ascribed to them in [F10regulation 8(1) of the Human Medicines Regulations 2012];

“unpackaged” (“heb ei becynnu”) means wholly or partly unwrapped.

Textual Amendments

Marginal Citations

M21984 c. 24; section 14 was substituted by S.I. 2005/2011, articles 2(1) and 6; and amended by S.I. 2007/3101, regulations 109 and 111.

M3S.I. 2008/1692, to which there are amendments not relevant to these Regulations.

M4S.I. 1992/662; relevant amending instruments are S.I. 2003/2624 (W. 252), S.I. 2007/205 (W. 19) and S.I. 2010/1647 (W.155).

M6S.I. 1972/1265 (N.I. 14), amended by 1978/1907 (N.I. 26); there are other amendments but none is relevant.

M71978 c. 29; there are amendments to section 27 which are not relevant to these Regulations.

M91968 c. 67; section 130 was amended by S.I. 1994/3119, regulation 2(b); and S.I. 2005/50, regulation 25(1)(c) and (d); there are other amendments but none is relevant.

M10S.I. 1997/1830; relevant amending instruments are S.I. 2003/696. S.I. 2004/1771, S.I. 2005/765, S.I. 2006/915, S.I. 2010/1621.