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Document 32001L0104
National transposition measures communicated by the Member States concerning:
Europa-Parlamentets og Rådets direktiv 2001/104/EF af 7. december 2001 om ændring af Rådets direktiv 93/42/EØF om medicinsk udstyr (EØS-relevant tekst)
OJ L 6, 10/01/2002, p. 50–51
(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. 25/2004 Sb., kterým se stanoví technické požadavky na zdravotnické prostředky
European Communities (Medical Devices) (Amendment) Regulations, 2002 SI n° 576 du 11/12/2002
Acte législatif n° 44006 du 30/04/2002 FEK B n° 577 du 09/05/2002, page 7695
Οι περί των Βασικών Απαιτήσεων (Ιατροτεχνολογικά Προϊόντα) Κανονισμοί του 2003
Medicīnisko ierīču un medicīnisko preču eksplutācijas un tehniskās uzraudzības kārtība
47/1999. (X. 6.) EüM rendelet az orvostechnikai eszközökről
Ustawa z dnia 20 kwietnia 2004 roku o wyrobach medycznych
Ustawa z dnia 20 maja 2010 r. o wyrobach medycznych
Decreto-Lei n° 30/2003 Diario da Republica I Serie A n° 38 du 14/02/2003 p. 986
Zákon č. 362/2011 Z. z. o liekoch a zdravotníckych pomôckach a o zmene a doplnení niektorých zákonov