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Post# A701218

Post Market Surveillance

Posted on: Thursday, 26 January, 2023  04:59
Updated On: Thursday, 26 January, 2023  05:00
Expires On: Wednesday, 22 October, 2025  10:59
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No matter how a medical device is classified, post-market surveillance is required and a manufacturer obligation. The company's quality management system (ISO 13485) should be connected with the post-market surveillance in order to assess data on the device's quality, functionality, and safety over the course of the device's whole lifecycle. Visit our website for more information about Post Market Surveillance.
http://www.i3cglobal.com/post-market-surveillance-report/ »

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