Medical Device Reporting

Views Updated: Dec 15, 2025

Key Facts

Abbreviation
MDR
Pronunciation
/ˈmɛdɪkəl dɪˈvaɪs rɪˈpɔrtɪŋ/
Category
Governmental
Related Field
FDA

Examples in Context

  1. These requirements include establishment registration, medical device listing, quality system, medical device reporting, premarket approval or clearance, labeling and U.S. agent requirements.
  2. Medical device adverse event reporting is an important basis for carrying out monitoring work of medical device, and it is also a primary means for evaluating the safety of listed products.
  3. And it develops the medical device adverse event on – line reporting system through using mixed survey procedure, step analysis, systematic analysis.
  4. Improvement of the medical device management through the suspicious harmful events reporting

Other meanings of MDR

Multi-Drug Resistance Medical
Multi-Drug Resistant Medical
miltidrug-resistant Medical
Multiple Drug Resistant Medical
Market Data Retrieval Business
Minimum Daily Requirement Misc
Marketing that Delivers Results Business
Mandatory Medical Device Reporting Gov
Milestone Decision Review Gov
Multiple Disease Resistance Medical