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CIRCULAR Type & number MDD Circular 00529 Date 11 June 2014 To Market Participants From MDD Coordinator Purpose For reviewMarket Domain Data Circular00529Page 0 of 711 June 2014 ELEXON 2024MDD change
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MDD Circular 00529 is a directive issued by regulatory authorities, outlining specific guidelines and requirements for the reporting and documentation of medical device data.
Manufacturers, importers, and distributors of medical devices that fall under the scope of the circular are required to file MDD Circular 00529.
To fill out MDD Circular 00529, entities must provide detailed information regarding their medical devices, including product descriptions, intended uses, compliance data, and any adverse event reports, using the prescribed format.
The purpose of MDD Circular 00529 is to enhance the monitoring and regulation of medical devices by ensuring accurate reporting and compliance with safety and efficacy standards.
Information that must be reported on MDD Circular 00529 includes device identification, manufacturer details, production data, safety information, and any changes to previously filed data.
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