Device-specific guidance for manufacturers on reporting adverse incidents under the European vigilance system To be read in conjunction with the European Commission’s guidelines on a medical devices vigilance system ME - Neurostimulator - Document - PDFSEARCH.IO

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	Device-specific guidance for manufacturers on reporting adverse incidents under the European vigilance system To be read in conjunction with the European Commission’s guidelines on a medical devices vigilance system ME Add to Reading List Document Date: 2013-08-15 04:59:25 Open Document File Size: 46,61 KB Share Result on Facebook Organization European Commission / / SocialTag Neurostimulator Rechargeable battery

Device-specific guidance for manufacturers on reporting adverse incidents under the European vigilance system To be read in conjunction with the European Commission’s guidelines on a medical devices vigilance system MEAdd to Reading List