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Anacreontic    
a. Anacreon风格的,饮酒谈情的,明朗的
n. Anacreon风格的诗

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  • Annex D: Cause Investigation – Investigation Conclusion
    Notes on using these codes: Wherever appropriate, the word 'device' should be interpreted as meaning all or any of the following: medical device, in-vitro diagnostic medical device, accessory to a medical device, medical device parts and or components
  • Terminologies for Categorized Adverse Event Reporting (AER): terms . . .
    As with the 2025 release, the 2026 release of the IMDRF terminology is a consolidated XLS workbook instead of a separate file for each annex Each annex is provided in a separate sheet within the main file The structure and layout of each annex sheet is unchanged from the last release
  • Coding Resources for Medical Device Reports | FDA
    Annex C: Added 1 new term (C23) and modified 1 term (C19) Annex D: Added 4 new terms (D0107, D0108, D1501, D18) and modified 3 terms (D10, D1107, D12)
  • MDR Adverse Event Codes | FDA
    This working group maintains a guidance document with seven annexes containing the IMDRF codes, which are posted to the IMDRF documents repository
  • Manage the IMDRF Dictionary | Veeva Vault Help
    To manage the IMDRF Device Code Dictionary, you must enable the IMDRF Dictionary for Maintenance, Case Processing, and Submissions To update the IMDRF Device Code Dictionary version: Navigate to Business Admin > Objects > Dictionaries > IMDRF Device Code Dictionary
  • IMDRF Code Lookup Tool — Search All 7 Annexes Free
    Search and browse IMDRF adverse event terminology codes across all 7 annexes Covers Device Problems, Patient Problems, Component Types, Cause Investigation, Health Effects, Investigation Types, and Investigation Findings Free and always up to date
  • IMDRF Codes: Meaning and Use in Medical Devices - VDE e. V.
    The terms and codes in Annex C are used to describe the results of the investigation, and the terms and codes in Annex D are used to describe the conclusions drawn from the investigations
  • New list of IMDRF Codes Published - MDSS
    The International Medical Device Regulators Forum (IMDRF) has released an updated version of its “Terminologies for Categorized Adverse Event Reporting (AER): Terms, Terminology and Codes” document
  • IMDRF Codes: The Key to Standardized Medical Device Data Management
    As an internationally standardized system, the IMDRF codes ensure clear communication between medical device manufacturers and regulatory authorities They provide the basis for transparency and cooperation on a global scale But how are the codes structured? What is the content behind them?





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