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16012479OMB APPROVAL
OMB Number:
32350123
Expires:
March 31, 2016,
Estimated average burden
hours per response...... 12.00Washington,D.C. 20549ANNUAL AUDITED REPORT
FORM X17A5
PART III SEC FILE
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What is mdd yy?
MDD YY refers to Medical Device Directive Year and is a regulatory requirement for medical device manufacturers.
Who is required to file mdd yy?
Medical device manufacturers or companies selling medical devices in the market are required to file MDD YY.
How to fill out mdd yy?
MDD YY can be filled out by providing all relevant information about the medical device as per the regulatory guidelines.
What is the purpose of mdd yy?
The purpose of MDD YY is to ensure the safety and efficacy of medical devices before they are placed in the market for public use.
What information must be reported on mdd yy?
Information such as device classification, technical documentation, conformity assessment, labeling, and post-market surveillance must be reported on MDD YY.
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