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Document 32003L0012
National transposition measures communicated by the Member States concerning:
Komisjoni direktiiv 2003/12/EÜ, 3. veebruar 2003, rinnaimplantaatide ümberliigitamise kohta meditsiiniseadmeid käsitleva direktiivi 93/42/EMÜ raamesEMPs kohaldatav tekst.
OJ L 28, 04/02/2003, p. 43–44
(ES, DA, DE, EL, EN, FR, IT, NL, PT, FI, SV) This document has been published in a special edition(s)
(CS, ET, LV, LT, HU, MT, PL, SK, SL, BG, RO, HR)
The member states bear sole responsibility for all information on this site provided by them on the transposition of EU law into national law. This does not, however, prejudice the results of the verification by the Commission of the completeness and correctness of the transposition of EU law into national law as formally notified to it by the member states. The collection National transposition measures is updated weekly.
Nařízení vlády č. 54/2015 Sb., o technických požadavcích na zdravotnické prostředky
Décret Présidentiel 3084.00/014/A/7825 du 17/12/2003 FEK n° 5 du 8/1/2004 p. 23
Attuazione della direttiva 2003/12/CE concernente la riclassificazione delle protesi mammarie.
Attuazione della direttiva 2003/12/CE concernente la riclassificazione delle protesi mammarie.
Οι Περί των Βασικών Απαιτήσεων (Ιατροτεχνολογικά Προϊόντα) Τροποποιητικοί Κανονισμοί του 2005.
47/1999. (X. 6.) EüM rendelet az orvostechnikai eszközökről
L.N. 210 of 2008 PRODUCT SAFETY ACT (CAP. 427) Medical Devices Regulations, 2008
Ustawa z dnia 20 kwietnia 2004 roku o wyrobach medycznych
Ustawa z dnia 20 maja 2010 r. o wyrobach medycznych
Decreto-Lei n° 259/2003 de 21 de outubro Diario da Republica I Serie A n° 244 de 21/10/2003 p. 7031
Consumer Protection -The Medical Devices (Amendment) Regulations 2003. SI n° 1697 of 4/7/2003