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MED2014016 Medical Directive Title: Use of Automated External Defibrillation in ResuscitationSleep Lab Lead Contact Person: Dawn Uruk, Coordinator Family Medical Centers and Sleep and Apnea Assessment
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Indicate the purpose of the form by explaining why you need the med-2014-016 - aed. Specify if it is for personal use, medical reasons, or any other purpose.
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If applicable, provide information about the patient or individual who will be using the AED (Automated External Defibrillator). Include their name, contact details, and any relevant medical information.
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Provide information about any training or certification you or your organization have received in the use of AEDs. Mention any relevant dates, certifications, or licenses.
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What is med-016 - aed for?
It is used for reporting adverse events related to medical devices.
Who is required to file med-016 - aed for?
Healthcare providers and manufacturers of medical devices are required to file med-016 - aed.
How to fill out med-016 - aed for?
Users can fill out med-016 - aed form electronically or manually, providing details of the adverse event.
What is the purpose of med-016 - aed for?
The purpose of med-016 - aed is to monitor and track adverse events related to medical devices for safety monitoring purposes.
What information must be reported on med-016 - aed for?
Information such as patient details, device information, adverse event description, and follow-up actions must be reported on med-016 - aed.
When is the deadline to file med-016 - aed for in 2023?
The deadline to file med-016 - aed for in 2023 is December 31st.
What is the penalty for the late filing of med-016 - aed for?
The penalty for late filing of med-016 - aed may include fines or suspension of the medical device license.
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