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Contact details for Guideline 8.04 Recall, Adverse Event And Post- Marketing Vigilance Reporting Of Medical Devices And IVDs

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28 Jan Contact details for Guideline 8.04 Recall, Adverse Event And Post- Marketing Vigilance Reporting Of Medical Devices And IVDs

Posted at 13:53h in by

2021 Dec

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Document Number: 8.04
Version: 1
Date Updated: 09/12/2021
File Type: pdf
Category: Communication to industry
Unit: Medical Devices