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Document 22004D0072
2004/72/: Decision of the EEA Joint Committee No 72/2004 of 8 June 2004 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement
2004/72/: Decision of the EEA Joint Committee No 72/2004 of 8 June 2004 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement
2004/72/: Decision of the EEA Joint Committee No 72/2004 of 8 June 2004 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement
OJ L 349, 25.11.2004, p. 29–29
(ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, NL, PL, PT, SK, SL, FI, SV) This document has been published in a special edition(s)
(BG, RO, HR)
OJ L 269M, 14.10.2005, p. 13–13
(MT)
In force
Relation | Act | Comment | Subdivision concerned | From | To |
---|---|---|---|---|---|
Modifies | 21994A0103(52) | Addition | chapter XXX point 5 | 09/06/2004 |
25.11.2004 |
EN |
Official Journal of the European Union |
L 349/29 |
DECISION OF THE EEA JOINT COMMITTEE
No 72/2004
of 8 June 2004
amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement
THE EEA JOINT COMMITTEE,
Having regard to the Agreement on the European Economic Area, as amended by the Protocol adjusting the Agreement on the European Economic Area, hereinafter referred to as ‘the Agreement’, and in particular Article 98 thereof,
Whereas:
(1) |
Annex II to the Agreement was amended by the Agreement on the participation of the Czech Republic, the Republic of Estonia, the Republic of Cyprus, the Republic of Hungary, the Republic of Latvia, the Republic of Lithuania, the Republic of Malta, the Republic of Poland, the Republic of Slovenia and the Slovak Republic in the European Economic Area signed on 14 October 2003 in Luxembourg (1). |
(2) |
Commission Directive 2003/32/EC of 23 April 2003 introducing detailed specifications as regards the requirements laid down in Council Directive 93/42/EEC with respect to medical devices manufactured utilising tissues of animal origin (2) is to be incorporated into the Agreement, |
HAS DECIDED AS FOLLOWS:
Article 1
The following point shall be inserted after point 4 (Commission Directive 2003/12/EC) in Chapter XXX of Annex II to the Agreement:
‘5. |
32003 L 0032: Commission Directive 2003/32/EC of 23 April 2003 introducing detailed specifications as regards the requirements laid down in Council Directive 93/42/EEC with respect to medical devices manufactured utilising tissues of animal origin (OJ L 105, 26.4.2003, p. 18).’ |
Article 2
The texts of Directive 2003/32/EC in the Icelandic and Norwegian languages, to be published in the EEA Supplement to the Official Journal of the European Union, shall be authentic.
Article 3
This Decision shall enter into force on 9 June 2004, provided that all the notifications pursuant to Article 103(1) of the Agreement have been made to the EEA Joint Committee (*1).
Article 4
This Decision shall be published in the EEA Section of, and in the EEA Supplement to, the Official Journal of the European Union.
Done at Brussels, 8 June 2004.
For the EEA Joint Committee
The President
S. GILLESPIE
(1) OJ L 130, 29.4.2004, p. 3.
(2) OJ L 105, 26.4.2003, p. 18.
(*1) No constitutional requirements indicated.