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This is a preview click here to buy the full publication IEC 60601263 Edition 1.0 201209 INTERNATIONAL STANDARD NORM INTERNATIONALE color inside Medical electrical equipment Part 263: Particular requirements
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What is iec 60601-2-63 - form?
The iec 60601-2-63 form is a specific form used for reporting medical device incidents.
Who is required to file iec 60601-2-63 - form?
Manufacturers, importers, and distributors of medical devices are required to file the iec 60601-2-63 form.
How to fill out iec 60601-2-63 - form?
The iec 60601-2-63 form can be filled out electronically or manually, following the guidelines provided by the regulatory authorities.
What is the purpose of iec 60601-2-63 - form?
The purpose of the iec 60601-2-63 form is to track and monitor medical device incidents to ensure patient safety.
What information must be reported on iec 60601-2-63 - form?
The iec 60601-2-63 form requires information such as the type of device, incident description, patient harm caused, and corrective actions taken.
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