This document is an excerpt from the EUR-Lex website
Document 32005L0050
National transposition measures communicated by the Member States concerning:
Kommissionens direktiv 2005/50/EG av den 11 augusti 2005 om omklassificering av höftleds-, knäleds- och axelledsproteser inom ramen för rådets direktiv 93/42/EEG om medicintekniska produkter (Text av betydelse för EES)
OJ L 210, 12/08/2005, p. 41–43
(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 287M, 18/10/2006, p. 294–296
(MT)
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
Verordnung zur Änderung medizinprodukterechtlicher Vorschriften
Meditsiiniseadmete liigitamise reeglid1
Meditsiiniseadmete liigitamise reeglid1
Εναρμόνιση της Ελληνικής νομοθεσίας προς την κοινοτική οδηγία 2005/50/ΕΚ....
Οι περί Βασικών Απαιτήσεων (Ιατροτεχνολογικά Προϊόντα) (Τροποποιητικοί) Κανονισμοί του 2007.
Az egészségügyi miniszter 16/2006. (III. 27.) EüM rendelete az orvostechnikai eszközökről
L.N. 113 of 2007 PRODUCT SAFETY ACT (CAP. 427) Medical Devices (Amendment) Regulations, 2007
L.N. 210 of 2008 PRODUCT SAFETY ACT (CAP. 427) Medical Devices Regulations, 2008
Ustawa z dnia 20 maja 2010 r. o wyrobach medycznych
Pravilnik o spremembah in dopolnitvah Pravilnika o medicinskih pripomočkih
Pravilnik o medicinskih pripomočkih
Föreskrifter om ändring i Läkemedelsverkets föreskrifter om medicintekniska produkter
The Medical Devices (Amendment) Regulations 2007