Regulation on Medical DevicesOfficial Journal Date : 9.01.2007
Official Journal Number : 26398
The objective of this Regulation is to lay down the essential requirements in vitro diagnostic medical devices and their accessories must meet and to establish the principles and procedures
relating to their design, classification, manufacture, placing on the market, putting into service and inspection for the purpose of providing safeguard measures for patients, appliers, users
and third parties against possible hazards they may be exposed to as regards their heath and safety during the use of such devices and their accessories. English translation of this legislation is not available, but can be provided upon request. If you would like to have up-to-dated English translation of this legislation (details of which is given above), Tariff-Tr.com team will be glad to help you. Please fill-in the form on the right to get a quotation from Tariff-Tr.com. We will send you an email describing the price, time for delivery, payment conditions and other details about your quotation. |
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