Obelis European Authorized Representative Center
"CE Marking Consultants with a Reputation for Excellence"4. Member States may require the information, which must be made available to the user and the patient in accordance with Annex I, point 13, to be in their national language(s) or in another Community language, when a device reaches the final user, regardless of whether it is for professional or other use. for a complete copy of the Directive, click here
Last updated Nov 10, 2008
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