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Vicon MX Hardware System Reference E-1
E
ERegulatory Notices
This appendix provides required regulatory notices regarding the
supply and use of Vicon MX in the United Kingdom and in the United
States of America:
MHRA Reporting Adverse Incidents on page E-2
FDA Medical Device Reporting System—Reportable Events on
page E-6
MXhardware_Reference.book Page 1 Monday, April 30, 2007 1:56 PM
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