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Clinical Trial Facilitation Group (CFTG) - Question and answers to the safety in clinical trials (04/03/2014) application/pdf
Post CE marketing market survey : the French experience on peracetic acid products used for material devices manual disinfection (juillet/04) - Competent authorities meeting on medical devices - Rotterdam (23/04/2008) application/pdf
Antimicrobial Susceptibility Testing, a new item in the field of european standardisation (25/04/2008) application/pdf
Guidelines on instruction for use of Troponin I/T cardiac marker devices (02/04/2008) application/pdf
Recommendations on evaluation of Troponin I/T cardiac marker devices (02/04/2008) application/pdf
Instructions for use (IFU) for medical devices (02/12/2009) application/pdf
List of essential medical devices in the event of a major health crisis: influenza pandemic scenario (11/12/2009) application/pdf
Silicone filled breast implants manufactured by POLY IMPLANT PROSTHESE (PIP (01/04/2010) application/pdf
Information for women with PIP breast implants -Questions/answers (26/07/2010) application/pdf
Silicone gel breast implants from Poly Implant Prothèse (PIP) Company - Information (26/07/2010) application/pdf
Risk of entrapment of "big children" in medical bed rails - Notice to manufacturers (28/07/2010) application/pdf
Medical "cot-beds" - regulations for manufacturing, import, export, marketing (free or for a price) and use (28/07/2010) application/pdf
Correct use of bed rails (11/08/2010) application/pdf
Decision determining specific conditions of use, putting into service, placing on the market, distribution, import and export, for the reinforcement of the safety of the children put in medical beds equipped with bed rails, (08/09/2010) application/pdf
Silicone filled breast implants from Poly Implant Prothèse Company Tests results - press release (28/09/2010) application/pdf
Pilot phase relative to the declaration of serious adverse events occurring during biomedical research concerning a medical device (24/11/2010) application/pdf
Notice to manufacturers of radiotherapy medical devices (22/05/2008) application/pdf
Formulaire de signalement de matériovigilance/réactovigilance et rapport fabricant - Report form/manufacturer's Incident report (11/06/2008) application/rtf
Communication of IIa, IIb, III class medical devices and AIMDD - explanatory note (24/06/2009) application/pdf
Procedure to allow delivery of non Class III separated elements articular prosthesis to partial replacements (12/02/2010) application/pdf
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