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Material Safety Data Sheet Product name : Revision : Print date : MD 535 Plaster remover Version : 15.10.2012 15.10.2012 5.0.0 01. Identification of the substance/preparation and of the company/undertaking
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What is durr md 535?
Durr MD 535 is a form used to report medical device adverse events to the Food and Drug Administration (FDA).
Who is required to file durr md 535?
Manufacturers, importers, and device user facilities are required to file durr MD 535.
How to fill out durr md 535?
Durr MD 535 can be filled out online through the FDA's MedWatch program or submitted via mail or fax.
What is the purpose of durr md 535?
The purpose of Durr MD 535 is to report adverse events and product problems related to medical devices.
What information must be reported on durr md 535?
Details of the adverse event, patient information, and the medical device involved must be reported on Durr MD 535.
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