This document is an excerpt from the EUR-Lex website
Document 32011L0100
National transposition measures communicated by the Member States concerning:
Komisijas Direktīva 2011/100/ES ( 2011. gada 20. decembris ), ar ko groza Eiropas Parlamenta un Padomes Direktīvu 98/79/EK par medicīnas ierīcēm, ko lieto in vitro diagnostikā Dokuments attiecas uz EEZ
OJ L 341, 22/12/2011, p. 50–51
(BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV) This document has been published in a special edition(s)
(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.
Bekendtgørelse om ændring af bekendtgørelse om medicinsk udstyr til in vitro-diagnostik
Verordnung über Medizinprodukte (Medizinprodukte-Verordnung MPV)
EM estime MNE non nécessaire - MS does not consider NEM necessary.
Meditsiiniseadmete liigitamise reeglid1
European Communities (In Vitro Diagnostic Medical Devices) (Amendment) Regulations 2012
8/2003. (III. 13.) ESzCsM rendelet az in vitro diagnosztikai orvostechnikai eszközökről
SUBSIDIARY LEGISLATION 427.16 IN VITRO DIAGNOSTIC MEDICAL DEVICES REGULATIONS
In Vitro Diagnostic Medical Devices (Amendment))Regulations, 2012
Verordnung, mit der die Verordnung über die Klassifizierung von Medizinprodukten geändert wird
Pravilnik o spremembi in dopolnitvi Pravilnika o medicinskih pripomočkih
The Medical Devices (Amendment) Regulations 2012