Traduction de «Medical Devices Unit » (Anglais → Français) :

medical device [ biomedical device | biomedical equipment | implant | medical and surgical instruments | medical apparatus | medical appliance | medical equipment | medical instrument | medical scanner | prosthesis | surgical device | surgical instrument | surgical material | therapeutic equipment | Medical and surgical equipment(ECLAS) | Medical technology(STW) | medical supplies(UNBIS) ]

devising medical device test procedures | medical device test procedures devising | develop medical device test procedures | medical device test procedure developing

testing a medical device | try medical devices | test a medical device | test medical devices

medical device testing methods | test procedures for medical devices | medical device test procedures | procedures for testing medical devices

accessory for a medical device | accessory to a medical device

active implantable medical device | active implanted medical device | AIMD [Abbr.]

device used for in vitro diagnosis | in vitro diagnostic medical device

unit record device [ unit record machine | tabulating device ]

basic device unit

Quantities of animal tissues or derivatives required to produce one unit of the medical device

Philippe Juvin, Thomas Ulmer, Linda McAvan, Gilles Pargneaux, Corinne Lepage, Antonyia Parvanova, Margrete Auken, Michèle Rivasi, Marina Yannakoudakis, Marisa Matias, Oreste Rossi (O-000101/2012 - B7-0118/2012) Group of the European People's Party (Christian Democrats) Group of the Progressive Alliance of Socialists and Democrats in the European Parliament Group of the Alliance of Liberals and Democrats for Europe Group of the Greens/European Free Alliance European Conservatives and Reformists Group Confederal Group of the European United Left - Nordic Green Left Europe of freedom and democracy Group Commission Defective silicone gel bre ...[+++]ast implants made by French company PIP: revision of EU legislation on medical devices

France and the United Kingdom requested the classification of total joint replacements as class III medical devices by way of derogation from the provisions of Annex IX to Directive 93/42/EEC, in order to ensure an appropriate conformity assessment of total joint replacements before their placing on the market.

The Commission is deeply committed to ensuring that high risk patient groups, and in particular infants in intensive care units, receive proper care and treatment delivered by safe medical devices.