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<bill bill-stage="Introduced-in-House" bill-type="olc" dms-id="H3D3B2402D14F4BF9A0E2AF5D11F1F463" public-private="public">
<metadata xmlns:dc="http://purl.org/dc/elements/1.1/">
<dublinCore>
<dc:title>110 HR 2791 IH: To amend the Federal Food, Drug, and Cosmetic Act to
</dc:title>
<dc:publisher>U.S. House of Representatives</dc:publisher>
<dc:date>2007-06-20</dc:date>
<dc:format>text/xml</dc:format>
<dc:language>EN</dc:language>
<dc:rights>Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.</dc:rights>
</dublinCore>
</metadata>
	<form>
		<distribution-code display="yes">I</distribution-code>
		<congress>110th CONGRESS</congress>
		<session>1st Session</session>
		<legis-num>H. R. 2791</legis-num>
		<current-chamber>IN THE HOUSE OF REPRESENTATIVES</current-chamber>
		<action>
			<action-date date="20070620">June 20, 2007</action-date>
			<action-desc><sponsor name-id="H000762">Ms. Hooley</sponsor> (for
			 herself and <cosponsor name-id="D000482">Mr. Doyle</cosponsor>) introduced the
			 following bill; which was referred to the <committee-name committee-id="HIF00">Committee on Energy and
			 Commerce</committee-name></action-desc>
		</action>
		<legis-type>A BILL</legis-type>
		<official-title>To amend the Federal Food, Drug, and Cosmetic Act to
		  provide for establishment of a unique device identification system for medical
		  devices.</official-title>
	</form>
	<legis-body id="HAC56E727DDC94C72B86FFD00F07F00D9" style="OLC">
		<section id="HD8917CEC1D0A4932AF23BDBF80D05D3" section-type="section-one"><enum>1.</enum><header>Short title</header><text display-inline="no-display-inline">This Act may be cited as the <quote>Unique
			 Device Identification System for Medical Devices Act of 2007</quote>.</text>
		</section><section id="H2860AD631F9542A2A4B725853EE2FDED"><enum>2.</enum><header>Unique device
			 identification system</header><text display-inline="no-display-inline">Section
			 519 of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/360i">21 U.S.C. 360i</external-xref>) is
			 amended—</text>
			<paragraph id="H495C3F224F2F45D286EAD3BCCFC7C037"><enum>(1)</enum><text>by redesignating
			 subsection (f) as subsection (g); and</text>
			</paragraph><paragraph id="HF16915FF603C426300F2E5ED697D8B21"><enum>(2)</enum><text>by inserting after
			 subsection (e) the following:</text>
				<quoted-block display-inline="no-display-inline" id="H88CF2B538BDF40209683D89FF71263D" other-style="archaic" style="other">
					<subsection id="H15A132D73A2846F4A9BF28D8A2F00F7"><enum>(f)</enum><header>Unique device identification system</header><text>The Secretary shall
				promulgate regulations establishing a unique device identification system for
				medical devices requiring the labeling of devices to bear a unique identifier.</text>
					</subsection><after-quoted-block>.</after-quoted-block></quoted-block>
			</paragraph></section></legis-body>
</bill>


