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	<id>https://wiki.dirkjanswagerman.nl/index.php?action=history&amp;feed=atom&amp;title=CFR_21-803_-_Medical_Device_Reporting</id>
	<title>CFR 21-803 - Medical Device Reporting - Revision history</title>
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	<updated>2026-10-25T11:27:36Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wiki.dirkjanswagerman.nl/index.php?title=CFR_21-803_-_Medical_Device_Reporting&amp;diff=493&amp;oldid=prev</id>
		<title>Dirkjan: Created page with &quot;These regulations implement the FDA&#039;s criteria for and authority requiring manufacturers, users and distributors to report health-related medical device failures and their cor...&quot;</title>
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		<updated>2020-08-25T07:18:12Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;These regulations implement the FDA&amp;#039;s criteria for and authority requiring manufacturers, users and distributors to report health-related medical device failures and their cor...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;These regulations implement the FDA&amp;#039;s criteria for and authority requiring manufacturers, users and distributors to report health-related medical device failures and their corrections or removal from the market. 21 CFR 803 is an important regulation for devices that may have health-related failures&lt;br /&gt;
[[Category:fda]]&lt;br /&gt;
&lt;br /&gt;
[[Category:CFR]]&lt;/div&gt;</summary>
		<author><name>Dirkjan</name></author>
		
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