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(1) These Regulations may be cited as the Medical Devices (Amendment) Regulations 2003 and shall come into force—
(a) except for the purposes of regulations 3(b), 6, 7 and 9, on 1st September 2003; and
(b) for the purposes of regulations 3(b), 6, 7 and 9, on 1st April 2004.
(2) In these Regulations, the  “principal Regulations” means the Medical Devices Regulations 2002 .
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In regulation 2(1) of the principal Regulations (interpretation)—
(a) the words  “, unless the context otherwise requires” are omitted;
(b) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(c) after the definition of  “Directive 2001/83”, there is inserted the following definitions—““Directive 2003/12” means Commission Directive 2003/12  of 3rd February 2003 on the reclassification of breast implants in the framework of Directive 93/42/EEC concerning medical devices;...”;
(d) in the definition of  “the Medical Devices Directives”, after  “Directive 93/42” there is inserted “
                , read with Directive 2003/32
              ”;
(e) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(f) in the definition of  “notified body”, for  “Part V of” there is substituted “
                Part V or
              ”; and
(g) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
3 
In regulation 4 of the principal Regulations (transitional provisions)—
(a) after paragraph (4) there is inserted the following paragraph—“
(5) Regulation 13(4) shall not be applied before 1st March 2004 in respect of breast implants which—
(a) bore a CE marking before 1st September 2003; and
(b) satisfy the requirements in respect of relevant devices falling within Class IIb set out in regulation 13(3).”; and
(b) after paragraph (5) there shall be added the following paragraph—“
(6) Regulation 19A shall not be applied before 1st October 2004 in respect of a device placed on the market before 1st April 2004.”.
4 
In regulation 5(1) and (2) of the principal Regulations (interpretation of Part II), the words  “, unless the context otherwise requires” are omitted.
5 
In regulation 7 of the principal Regulations (classification of general medical devices), after  “Directive 93/42”, at both places where this occurs, there is inserted “
            , read with Directive 2003/12
          ”.
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8 
In regulation 18 of the principal Regulations (UK notified bodies and the conformity assessment procedures for general medical devices), after paragraph (3) there is added the following paragraph—“
(4) Decisions taken by UK notified bodies before 1st September 2003 in accordance with Annex II in respect of breast implants may not be extended.”.
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10 
In regulation 20 of the principal Regulations (interpretation of Part III)—
(a) in paragraphs (1) and (2) the words  “, unless the context otherwise requires” are omitted;
(b) in paragraph (2), the words  “article or”, at both places where they occur, are omitted.
11 
In regulation 32(1) and (2) of the principal Regulations (interpretation of Part IV), the words  “, unless the context otherwise requires” are omitted.
12 
In Part V of the principal Regulations (notified bodies, conformity assessment bodies and marking of products), before regulation 45 (designation etc. of UK notified bodies) there is inserted the following regulation—“
44A 
In this Part,  “medical device” means a device that is a  “relevant device” for the purposes of Part II, III or IV.”.
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15 
In regulation 52(1) of the principal Regulations (interpretation of Part VI), the words  “, unless the context otherwise requires” are omitted.
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17 
In regulation 59 of the principal Regulations (interpretation of Part VII), the words  “, unless the context otherwise requires” are omitted.
 Signed by authority of the Secretary of State for Health
Warner
Parliamentary Under-Secretary of State,
Department of Health
