This document is an excerpt from the EUR-Lex website
Document 32003L0032
National transposition measures communicated by the Member States concerning:
Direktiva Komisije 2003/32/EZ od 23. travnja 2003. o uvođenju detaljnih specifikacija u pogledu zahtjeva utvrđenih u Direktivi Vijeća 93/42/EEZ u odnosu na medicinske proizvode proizvedene korištenjem tkiva životinjskog podrijetla Tekst značajan za EGP
OJ L 105, 26/04/2003, p. 18–23
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Zákon č. 22/1997 Sb., o technických požadavcích na výrobky a o změně a doplnění některých zákonů
Meditsiiniseadme vastavushindamise kord1
Zakon o medicinskim proizvodima
Pravilnik o posebnim zahtjevima za medicinske proizvode izrađene od neživog životinjskog tkiva
L.N. 210 of 2008 PRODUCT SAFETY ACT (CAP. 427) Medical Devices Regulations, 2008
Besluit van 26 april 2004, houdende wijziging van het Besluit medische hulpmiddelen
Aanwijzing KEMA Quality B.V. als uitvoeringsinstatie o.g.v. Besluit medische hulpmiddelen.
Ustawa z dnia 20 kwietnia 2004 roku o wyrobach medycznych
Ustawa z dnia 20 maja 2010 r. o wyrobach medycznych
Pravilnik o spremembah in dopolnitvah pravilnika o medicinskih pripomočkih
Consumer Protection -The Medical Devices (Amendment) Regulations 2003. SI n° 1697 of 4/7/2003