MAUDE brand profile

BAND 620BG23 DURAN ANCORE ANNULOPLASTY C

MAUDE brand safety profile

Key facts

Brand name BAND 620BG23 DURAN ANCORE ANNULOPLASTY C

At a glance

  • 10–99 MAUDE reports
  • 1–9 Death reports
  • 1–9 Injury reports
  • 10–99 Problems coded
  • 10–99 Problems flagged by Orca1 signal analytics
  • Mitral Regurgitation, Adverse Event Without Identified Device or Use Problem, Insufficient Information, Mitral Valve Stenosis, Thromboembolism, No Information, Mitral Valve Prolapse, Structural Problem Most reported problems

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About MAUDE brand safety profiles

Brand profiles aggregate every MAUDE report that names the brand, so you can compare report volumes and problem patterns across devices. Reports are unverified and do not by themselves establish causation.

Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1

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