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Form DSA 1-MR is a form used to report certain information related to medical devices.
Manufacturers, importers, and distributors of medical devices are required to file Form DSA 1-MR.
Form DSA 1-MR can be filled out electronically or manually, following the instructions provided by the regulatory authority.
The purpose of form DSA 1-MR is to ensure that medical devices in the market meet the necessary regulatory requirements for safety and efficacy.
Form DSA 1-MR typically requires information such as device details, manufacturing information, importation details, and distribution information.
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