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AIMD
Accessory for a medical device
Accessory to a medical device
Active implantable medical device
Active implanted medical device
Biomedical device
Biomedical equipment
Canada's Medical Device Technology Companies
Canada's Medical Technology Companies
Develop medical device test procedures
Device used for in vitro diagnosis
Devising medical device test procedures
Implant
In vitro diagnostic medical device
In-Vitro Diagnostic Medical Devices directive
MEDEC
Medical Devices Canada
Medical and surgical equipment
Medical and surgical instruments
Medical apparatus
Medical appliance
Medical device
Medical device monitoring
Medical device reporting
Medical device surveillance
Medical device test procedure developing
Medical device test procedures
Medical device test procedures devising
Medical device testing methods
Medical device vigilance
Medical equipment
Medical instrument
Medical scanner
Medical supplies
Medical technology
Procedures for testing medical devices
Prosthesis
Surgical device
Surgical instrument
Surgical material
Test a medical device
Test medical devices
Test procedures for medical devices
Testing a medical device
Therapeutic equipment
Try medical devices

Translation of "medical devices canada " (English → French) :

TERMINOLOGY
see also In-Context Translations below
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) ]

matériel médical [ appareil médical | dispositif médical | équipement biomédical | équipement médical | équipement thérapeutique | implant | instrument médical | matériel biomédical | matériel chirurgical | matériel médico-chirurgical | prothése | scanner médical ]


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

élaborer des procédures d’essai de dispositifs médicaux


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

tester des dispositifs médicaux


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

procédures d’essai de dispositifs médicaux


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

dispositif médical implantable actif


accessory for a medical device | accessory to a medical device

accessoire de dispositif médical


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

dispositif destiné au diagnostic in vitro | dispositif médical de diagnostic in vitro


Canada's Medical Technology Companies [ MEDEC | Medical Devices Canada | Canada's Medical Device Technology Companies | Canadian Association of Manufacturers of Medical Devices ]

Les Sociétés canadiennes de technologies médicales [ MEDEC | Instruments médicaux Canada | Association canadienne des fabricants d'équipement médical ]


medical device reporting [ medical device vigilance | medical device monitoring | medical device surveillance ]

matériovigilance


Directive 98/79/EC on in vitro diagnostic medical devices [ Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices | In-Vitro Diagnostic Medical Devices directive ]

Directive relative aux dispositifs médicaux de diagnostic in vitro [ Directive 98/79/CE du Parlement européen et du Conseil, du 27 octobre 1998, relative aux dispositifs médicaux de diagnostic in vitro ]
IN-CONTEXT TRANSLATIONS
WHEREAS medical device problem reporting is an essential element in the continued efforts of the Health Products and Food Branch Inspectorate of the Department of Health to protect the health and safety of Canadians; AND WHEREAS, although manufacturers and importers are required to report certain medical device problems, the Parliament of Canada acknowledges that a complementary medical device problem notification system should be maintained by the Department of Health; NOW, THEREFORE, Her M ...[+++]

Attendu : que la déclaration des défectuosités des instruments médicaux fait partie intégrante des efforts constants que déploie l'Inspectorat de la Direction générale des produits de santé et des aliments du ministère de la Santé pour protéger la santé des Canadiens et assurer leur sécurité; que, bien que les fabricants et les importateurs soient tenus de signaler certaines défectuosités des instruments médicaux, le Parlement du Canada est d'avis que le ministère de la Santé devrait gérer un système complémentaire de déclaration des ...[+++]


Its participating regions (US, EU, Canada, Japan, Australia, Brazil, China and Russia) recently endorsed key definitions for software that are medical devices.

Ses régions participantes (États-Unis, UE, Canada, Japon, Australie, Brésil, Chine et Russie) ont récemment approuvé d'importantes définitions concernant les logiciels qui constituent des dispositifs médicaux.


Corrective contact lenses are classified and regulated as medical devices under the Food and Drugs Act and are regulated as class II medical devices by Health Canada.

Les lentilles correctrices sont considérées comme des instruments médicaux en vertu de la Loi sur les aliments et drogues et sont réglementées comme tels.


Under the current regulatory regimes and in keeping with the federal constitutional jurisdiction, Health Canada has legislative authorities in place to regulate the safety and effectiveness of medical devices and their manufacturers under the Food and Drugs Act and the medical devices regulations.

En vertu des régimes de réglementation actuels et dans le cadre des compétences conférées au gouvernement fédéral par la Constitution, Santé Canada est déjà investi de l'autorité législative nécessaire pour réglementer la sécurité et l'efficacité des instruments médicaux et leurs fabricants en vertu de la Loi sur les aliments et drogues et des règlements relatifs aux instruments médicaux.


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The use of DEHP in medical devices was reviewed by the Medical Devices Bureau of Health Canada.

L'utilisation du DEHP dans les instruments médicaux a fait l'objet d'un examen par le Bureau des matériels médicaux de Santé Canada.


Your committee has heard that Health Canada currently has the necessary authorities in place to adequately regulate medical devices through the Medical Devices Regulations under the Food and Drugs Act.

Votre comité a entendu que Santé Canada possède déjà les pouvoirs requis afin de réglementer adéquatement les instruments médicaux en appliquant le Règlement sur les instruments médicaux pris en vertu de la Loi sur les aliments et drogues.




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Date index: 2024-03-07
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