Medical Device Advisory Notice
September 15, 2050
[RECIPIENT'S NAME]
[RECIPIENT'S ADDRESS]
Dear [RECIPIENT'S NAME],
We are writing to inform you about some important updates and guidelines for your medical device(s). This advisory notice is issued in light of recent updates from medical device regulators. You must follow these instructions to ensure the safety and effectiveness of the medical equipment you are using.
Under the latest Medical Device Regulations (MDR), we want to emphasize that all devices should comply with device registration, labeling, packaging, and, if applicable, tracking requirements. Any discrepancy found in these elements may cause non-compliance with legal regulations, which may lead to penal consequences.
This advisory also includes stern instructions to abstain from any modifications or adjustments to the device unless instructed by a licensed professional or authorized person from the manufacturer. Tampering with the device's original aspect can result in unexpected performance issues or could potentially render the device unsafe.
In case of any malfunction or abnormality detected during operation, stop using the device immediately and report to the closest medical center or call our support team at [YOUR COMPANY NUMBER] for further advice. We highly encourage you to adhere to this guideline and seek advice from healthcare professionals for further details.
Please do not hesitate to contact us at [YOUR EMAIL] for more information or clarification. Thank you for your understanding and compliance with this advisory notice. Your safety and health are our paramount concern.
Sincerely,
[YOUR NAME]
[YOUR COMPANY NAME]
[YOUR COMPANY ADDRESS]
[YOUR COMPANY NUMBER]
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