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Get the free Urgent Medical Device Correction - 2955842-03/16/16-005-C

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Date : 14 Apr 2016Field Safety Notice Urgent Medical Device Correction 295584203/16/16005C Proper use of da Vinci S, Si, and Xi Instruments for Manipulation of Cryoablation Probes in Cardiac Procedures
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Identify the urgent medical device correction notice received.
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Review the instructions provided in the notice.
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Fill out the necessary information on the correction form or document.
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Provide any required documentation or evidence related to the correction.
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Submit the completed form or document according to the instructions provided.

Who needs urgent medical device correction?

01
Medical device manufacturers
02
Healthcare facilities
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Healthcare providers
04
Patients who are using the medical device requiring correction
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Urgent medical device correction is a process to address serious safety concerns with a medical device that could potentially cause harm to patients or users.
Manufacturers, distributors, and importers of medical devices are required to file urgent medical device correction.
Urgent medical device correction forms can typically be filled out online through regulatory authorities or notified bodies.
The purpose of urgent medical device correction is to quickly address safety issues with medical devices to prevent harm to patients or users.
Information such as the description of the safety issue, affected product details, the scope of the correction, and the actions to be taken must be reported on urgent medical device correction.
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