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December 15, 2017, To:Surgeons/ HospitalsSubject:URGENT MEDICAL DEVICE FIELD SAFETY NOTICE (Removal)Reference:FA 201705 (ZFA2017404)Affected Product: REVIVAL MODULAR RASP DISTAL Credited Number 01.00409.612 01.00409.613 01.00409.614 01.00409.615 01.00409.616 01.00409.617 01.00409.622 01.00409.623 01.00409.624 01.00409.625 01.00409.626 01.00409.627 01.00409.628 01.00409.629 01.00409.633 01.00409.634 01.00409.635 01.00409.636 01.00409.637 01.00409.638 01.00409.639Product
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To fill out the urgent medical device field, follow these steps:
02
Start by accessing the medical device form or database where the field is located.
03
Look for the specific section or field designated for urgent medical devices.
04
Ensure you have all the necessary information and details about the device you want to report as urgent.
05
Enter the relevant information into the urgent medical device field. This may include device name, model number, serial number, and any specific urgent alerts or reasons for reporting.
06
Double-check the accuracy of the entered information before submitting.
07
Save or submit the form to record the urgent medical device information.
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If there are any additional steps or requirements specific to the medical device form or database, make sure to follow those as well.

Who needs urgent medical device field?

01
Anyone who has identified a medical device that requires urgent attention, such as immediate recall, safety concern, or malfunction, needs to fill out the urgent medical device field.
02
This field is crucial for healthcare professionals, medical device manufacturers, regulatory agencies, and other stakeholders involved in tracking and addressing urgent medical device issues.
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The urgent medical device field is a section where information about medical devices that require immediate attention due to safety concerns or performance issues is reported.
Manufacturers, importers, and device distributors are required to file the urgent medical device field when necessary.
The urgent medical device field must be filled out with detailed information about the medical device, the safety concerns or performance issues, and any actions taken by the manufacturer to address the problem.
The purpose of the urgent medical device field is to ensure that relevant authorities are informed about medical devices that pose a risk to patient safety so that appropriate actions can be taken.
Information such as the name of the device, manufacturer details, description of the safety concern or performance issue, and any corrective actions taken must be reported on the urgent medical device field.
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