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Medical Device Control Office Change Form for Listed Medical Devices:Medical Device Control Office (Fax No: 3157 1286)MDC Reference: AN(Attn:Secretary to MDL AB)Listing No: LRP Name: HKD No. Application
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The form medical device administrative is needed by individuals or organizations involved in the medical device industry.
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The Medical Device Administrative Form is a document required by regulatory authorities to ensure that medical devices meet safety and efficacy standards before they can be marketed or sold.
Manufacturers, importers, and distributors of medical devices are required to file the Medical Device Administrative Form.
To fill out the Medical Device Administrative Form, provide accurate information about the device, including its classification, intended use, manufacturer details, and compliance with applicable regulations.
The purpose of the Medical Device Administrative Form is to gather information that ensures the safety, reliability, and effectiveness of medical devices in the market.
The form requires reporting of device identification details, manufacturer information, device safety and effectiveness data, compliance with standards, and any adverse event history.
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