Übersetzung für "E 385 " (Englisch → Deutsch) :

calcium disodium ethylene diamine tetra-acetate | calcium disodium EDTA [ E 385 ]

e-administration (nom) | e-gov (nom) | e-Gov (nom) | eGovernment (nom) | e-government (nom) | e-Government (nom) | electronic administration (nom) | electronic government (nom) | electronic public administration (nom) | net government (nom) | online administration (nom) | on-line administration (nom) | online government (nom) | on-line government (nom)

(E) 7- (Z) 9-dodecadienyl acetate (1) | dodecadienylacetate- (E) 7- (Z) 9 (2) | dodecadienylacetate, e-7, z-9- (3)

e-human resources management (e-HRM)

E-learning | E-training | On-line training

spam | spam message | e-mail spam | junk e-mail | junk mail

otorhinolaryngology | E.N.T

cycloderma | no definition found (E)

In order to satisfy the legal requirements laid down in Directive 90/385/EEC, in Directive 93/42/EEC and in Directive 98/79/EC, notified bodies should verify, where relevant, the fulfilment of the essential safety and health requirements contained in Directive 2006/42/EC of the European Parliament and of the Council of 17 May 2006 on machinery, and amending Directive 95/16/EC , of the requirements contained in Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin and of the common technical specification ...[+++]s for in vitro diagnostic medical devices laid down in Commission Decision 2002/364/EC of 7 May 2002 on common technical specifications for in vitro diagnostic medical devices

1. Member States shall verify that bodies notified under Article 11 of Directive 90/385/EEC or Article 16 of Directive 93/42/EEC have up-to-date knowledge of the medical devices referred to in Article 1(1), in order to assess the conformity of those devices with the provisions of Directive 90/385/EEC or Directive 93/42/EEC, respectively, and with the particular requirements laid down in Annex I to this Regulation.

EUROPA - EU law and publications - EUR-Lex - EUR-Lex - 32012R0722 - EN - Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin Text with EEA relevance // COMMISSION REGULATION (EU) No 722/2012 // of 8 August 2012 // (Text with EEA relevance)

For clinical investigations Member States shall ensure that an extract of the notifications referred to in Article 10(1) of Directive 90/385/EEC and in Article 15(1) of Directive 93/42/EEC, as well as the information referred to in Article 10(3) and (4) of Directive 90/385/EEC and in Article 15(6) and (7) of Directive 93/42/EEC are entered into Eudamed in accordance with the Annex to this Decision.