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13MED040558 232201 K30946 06/12/2014 MASTER CONTRACT BETWEEN THE APPLEWOOD EDUCATION ASSOCIATION AND APPLEWOOD BOARD OF EDUCATIONSEPTEMBER 1, 2013 AUGUST 31, 2016TABLE OF CONTENTS PAGE ARTICLE I Section
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13-med-04-0558 is a form used for reporting medical device incidents.
Manufacturers, importers, and device user facilities are required to file 13-med-04-0558.
You can fill out 13-med-04-0558 online through the FDA's MedWatch website or by mailing a paper form.
The purpose of 13-med-04-0558 is to report adverse events or product problems related to medical devices.
Information such as the patient's name, contact information, device type, event description, and medical facility details must be reported on 13-med-04-0558.
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